Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_assertion description "[The b-wave of their photopic ERG was significantly more attenuated than the a-wave due to the specific abolition of OP4, while the amplitudes of OP2 and OP3 were within the normal range, giving to the b-wave a truncated appearance reminiscent of that seen in congenital stationary night blindness (CSNB) with myopia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_assertion evidence source_evidence_literature NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_assertion SIO_000772 10189180 NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_assertion wasDerivedFrom befree-20140225 NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_assertion wasGeneratedBy ECO_0000203 NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP323729.RAkHWBFhbrdPv_GxAO3gW1snxSTM_EGguUueTsxqFt6PI130_provenance.