Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_assertion description "[it is reported for the first time that mutations in CABP4 lead to autosomal recessive congenital stationary night blindness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_assertion evidence source_evidence_literature NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_assertion SIO_000772 16960802 NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_assertion wasDerivedFrom lhgdn-20090331 NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_assertion wasGeneratedBy ECO_0000203 NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP150795.RAz-9h7XHc4DsUqa_0i_1WaAcq8SO2NohQcMy5Nxa7ZGo130_provenance.