Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_assertion description "[Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_assertion evidence source_evidence_literature NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_assertion SIO_000772 18400204 NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_assertion wasDerivedFrom befree-2016 NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_assertion wasGeneratedBy ECO_0000203 NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.
- befree-2016 importedOn "2016-02-19" NP664976.RApAzsGeyf6pRcqBJXMpFoTc-Ailt5GqBmwXgXDMpFzDw130_provenance.