Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_assertion description "[Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_assertion evidence source_evidence_literature NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_assertion SIO_000772 12704386 NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_assertion wasDerivedFrom befree-20140225 NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_assertion wasGeneratedBy ECO_0000203 NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP427119.RAL5KjMwQAl1hGbfbrthq0rHI1mVzNFCOtuVY6IkA-_5g130_provenance.