Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_assertion description "[This was the first study to examine the associations of the PRKCH polymorphism with GA and GC, and suggested that the AA genotype, relative to the G/G genotype, may be a higher risk genotype for severe GA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_assertion evidence source_evidence_literature NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_assertion SIO_000772 20602195 NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_assertion wasDerivedFrom befree-2016 NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_assertion wasGeneratedBy ECO_0000203 NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.
- befree-2016 importedOn "2016-02-19" NP823637.RAbHRmjZIsVChgvFnhgcn8yTryAhWv2cqORO0K-CZA5lE130_provenance.