Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_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." NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_assertion evidence source_evidence_literature NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_assertion SIO_000772 17241866 NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_assertion wasDerivedFrom befree-20150227 NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_assertion wasGeneratedBy ECO_0000203 NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.
- befree-20150227 importedOn "2015-02-27" NP619080.RAbPeDN0V3pP1oj8tv4ugCc9l1yOUbNtPpjRH4rH0IKco130_provenance.