Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_assertion wasGeneratedBy ECO_0000203 NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_assertion wasDerivedFrom befree-20140225 NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_assertion SIO_000772 8045710 NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_assertion evidence source_evidence_literature NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_assertion description "[Patients from two families, one with a mutation in codon 167 (Gly167Asp) leading to macular degeneration and another with a mutation in codon 210 (Pro210Ser) leading to retinitis pigmentosa, were studied with clinical examinations and measurements of rod and cone sensitivities and dark adaptation, electroretinography, and rhodopsin levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP169747.RA0BMr7SwPktOmGcMH_OmJR4Wu4GVIpDhOexHGwAzt89c130_provenance.