Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_assertion description "[The genes for phosphatidylinositol transfer protein (PITPN), retinal guanylate cyclase (GUC2D), beta-arrestin 2 (ARRB2), pigment epithelium-derived factor (PEDF) and recoverin (RCV1) map to this region and are candidate genes for retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_assertion evidence source_evidence_literature NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_assertion SIO_000772 8733141 NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_assertion wasDerivedFrom befree-20150227 NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_assertion wasGeneratedBy ECO_0000203 NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP252672.RAe8wgCmc5KNkA1CWMTY79ZeaDtCCpY_7nnladceBaJKc130_provenance.