Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_assertion description "[Our results suggest that mutant alleles in RDH5 are a cause of fundus albipunctatus, a rare form of stationary night blindness characterized by a delay in the regeneration of cone and rod photopigments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_assertion evidence source_evidence_literature NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_assertion SIO_000772 10369264 NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_assertion wasDerivedFrom befree-20140225 NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_assertion wasGeneratedBy ECO_0000203 NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP643472.RAs1WHdr-ILzF5eFhq3yv1VaL8wmsmZCQay_mpoMqtjhE130_provenance.