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American_Journal
Documents
(145)
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# proj.
# Ann.
updated_at
PMC
4572498
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations Abstract We tested
42.5 KB
2021-06-04
3
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PMC
4572507
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease Abstract The Human Ph
50.1 KB
2021-06-04
3
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PMC
4572568
Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding
48.6 KB
2021-06-04
3
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PMC
4572578
Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy Abstract Acut
21.2 KB
2021-06-04
3
-
PMC
4573257
TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated
36.2 KB
2021-06-04
3
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PMC
4596892
Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp]
34.1 KB
2021-06-04
3
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PMC
4596894
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
35.3 KB
2021-06-04
3
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PMC
4596912
Alternative Splicing QTLs in European and African Populations Abstract With the advent of RNA-seque
40.1 KB
2021-06-04
3
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PMC
4596914
Imputation of KIR Types from SNP Variation Data Abstract Large population studies of immune system
65.8 KB
2021-06-04
3
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PMC
4667104
Amino Acid Variation in HLA Class II Proteins Is a Major Determinant of Humoral Response to Common V
21.5 KB
2021-06-04
3
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