Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_assertion description "[Mutations in RPGR account for over 70% of X-linked retinitis pigmentosa (XlRP), characterized by retinal degeneration and eventual blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_assertion evidence source_evidence_literature NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_assertion SIO_000772 21857984 NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_assertion wasDerivedFrom befree-20140225 NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_assertion wasGeneratedBy ECO_0000203 NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP655220.RAVa3SmOotRGzSbMEswZOZ1G5tgQ_xs-O2NMlURkM31PQ130_provenance.