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PubPharm (41)
1
The Medical Action Ontology: A Tool for Annotating and Analyzing Treatments and Clinical Management of Human Disease
enthalten in:
bioRxiv.org
| 2024
von
Carmody, L.
|
Gargano, M.
|
Toro, S.
| +23
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2
The Medical Action Ontology : A tool for annotating and analyzing treatments and clinical management of human disease
enthalten in:
Med (New York, N.Y.)
| 2023
von
Carmody, L.
|
Gargano, M.
|
Toro, S.
| +23
UpdateOf: medRxiv. 2023 Jul 13;:. - PMID 37503136
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3
The Medical Action Ontology : A Tool for Annotating and Analyzing Treatments and Clinical Management of Human Disease
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Carmody, L.
|
Gargano, M.
|
Toro, S.
| +23
UpdateIn: Med. 2023 Nov 9;:. - PMID 37963467
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4
Phenopacket-tools : Building and validating GA4GH Phenopackets
enthalten in:
PloS one
| 2023
von
Danis, D.
|
Jacobsen, J.
|
Wagner, A.
| +15
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5
Semantic Integration of Clinical Laboratory Tests from Electronic Health Records for Deep Phenotyping and Biomarker Discovery
enthalten in:
bioRxiv.org
| 2022
von
Zhang, X.
|
Yates, A.
|
Vasilevsky, N.
| +21
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6
Prenatal phenotyping : A community effort to enhance the Human Phenotype Ontology
enthalten in:
American journal of medical genetics. Part C, Seminars in medical genetics
| 2022
von
Dhombres, F.
|
Morgan, P.
|
Chaudhari, B.
| +33
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7
Mondo: Unifying diseases for the world, by the world
enthalten in:
bioRxiv.org
| 2022
von
Vasilevsky, N.
|
Matentzoglu, N.
|
Toro, S.
| +83
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8
A community effort for COVID-19 Ontology Harmonization
enthalten in:
CEUR workshop proceedings
| 2022
von
Lin, A.
|
Yamagata, Y.
|
Duncan, W.
| +9
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9
Prenatal phenotyping : A community effort to enhance the Human Phenotype Ontology
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2022
von
Dhombres, F.
|
Morgan, P.
|
Chaudhari, B.
| +33
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10
Interpretable prioritization of splice variants in diagnostic next-generation sequencing
enthalten in:
American journal of human genetics
| 2021
von
Danis, D.
|
Jacobsen, J.
|
Carmody, L.
| +7
ErratumFor: Am J Hum Genet. 2021 Sep 2;108(9):1564-1577. - PMID 34289339
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4
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4
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neurabin
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ontology
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2
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Congenital disorders of glycosylation
2
EC 2.5.1.18
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