Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_assertion description "[Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_assertion evidence source_evidence_literature NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_assertion SIO_000772 18445228 NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_assertion wasDerivedFrom befree-2016 NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_assertion wasGeneratedBy ECO_0000203 NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.
- befree-2016 importedOn "2016-02-19" NP668476.RAUPu6AmyiBF6J2y4bSG8d2T7uVnGwgJeFeIAZYau18t8130_provenance.