Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_assertion description "[Patients with mutations in the ATP6V1B1 proton pump subunit develop dRTA and in most of the cases sensorineural hearing loss early in childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_assertion evidence source_evidence_literature NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_assertion SIO_000772 22509993 NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_assertion wasDerivedFrom befree-20140225 NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_assertion wasGeneratedBy ECO_0000203 NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563760.RAZDMVJFbYTQvqQKqVE1ax6pBgxDsAKGb5bbGda8TNMMA130_provenance.