Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_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." NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_assertion evidence source_evidence_literature NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_assertion SIO_000772 17241866 NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_assertion wasDerivedFrom befree-20140225 NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_assertion wasGeneratedBy ECO_0000203 NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP673535.RAEK-9Qdxn-VSRLQMNfLiTt1UQZihd1Wr-xH6xbqdsUP4130_provenance.