Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_assertion description "[Inherited syndromes of intrahepatic cholestasis commonly result from mutations in the genes SERPINA1 (alpha(1)-antitrypsin deficiency), JAG1 (Alagille syndrome), ATP8B1 (progressive familial intrahepatic cholestasis type 1 [PFIC1]), ABCB11 (PFIC2), and ABCB4 (PFIC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_assertion evidence source_evidence_literature NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_assertion SIO_000772 17241866 NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_assertion wasDerivedFrom befree-2016 NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_assertion wasGeneratedBy ECO_0000203 NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.
- befree-2016 importedOn "2016-02-19" NP590032.RAhr8y1C60Dm7U0WX-9Ra6AOR4poQcMi0cVc-S5u2jADk130_provenance.