Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_assertion description "[IL28B polymorphism seems to be involved in the development of HCV-induced HCC and in the course of HCV recurrence after LT. T allele may be regarded as a genetic risk factor for HCV-related carcinogenesis, posttransplant fibrosis progression, and antiviral therapy failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_assertion evidence source_evidence_literature NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_assertion SIO_000772 22411462 NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_assertion wasDerivedFrom befree-2016 NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_assertion wasGeneratedBy ECO_0000203 NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.
- befree-2016 importedOn "2016-02-19" NP967152.RAsTAvQ3CJx1q6BOdSes4SLx6DQ5lPp7rfn1-KQx0UOyc130_provenance.