Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_assertion wasGeneratedBy ECO_0000203 NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_assertion wasDerivedFrom befree-20140225 NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_assertion SIO_000772 22735794 NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_assertion evidence source_evidence_literature NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_assertion description "[The aim of this study was to identify mutations in the TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindness (CSNB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241716.RAEnG6jqDJkNFSGZBFfJs8c36sGNNIIliX-9w-edHX0v0130_provenance.