Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_assertion description "[The results indicate that GNB3 and GNGT2 are unlikely sites of mutations responsible for inherited retinal degenerations that predominantly effect cone-mediated function (cone and cone-rod dystrophies) or have a predilection for disease in the macula (macular dystrophies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_assertion evidence source_evidence_literature NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_assertion SIO_000772 9743540 NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_assertion wasDerivedFrom befree-2016 NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_assertion wasGeneratedBy ECO_0000203 NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404240.RArEOG8sfkJ_SV4UaewaJ5CLnIlDkzRNBWkB4m2vHHW7Q130_provenance.