Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_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." NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_assertion evidence source_evidence_literature NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_assertion SIO_000772 17241866 NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_assertion wasDerivedFrom befree-20140225 NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_assertion wasGeneratedBy ECO_0000203 NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP802579.RAk6x47D09jNh9Daz2Q3Rjn4P_Hf23Y_RxArYms2ySbzc130_provenance.