Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_assertion description "[Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_assertion evidence source_evidence_literature NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_assertion SIO_000772 10982042 NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_assertion wasDerivedFrom befree-20140225 NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_assertion wasGeneratedBy ECO_0000203 NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP669506.RAlasUx8YDLUT-c0c6N8ndxii3TPkCLyUGV1nzviKR17w130_provenance.