Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_assertion description "[Mutations in RP2 cause the second most frequent form of X-linked retinitis pigmentosa, a severe retinal degeneration that leads to loss of visual acuity and blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_assertion evidence source_evidence_literature NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_assertion SIO_000772 11371510 NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_assertion wasDerivedFrom befree-20140225 NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_assertion wasGeneratedBy ECO_0000203 NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.
- befree-20140225 importedOn "2014-02-25" NP555121.RAnO7AHruG6ZYYrcSRSLlSst7FTDfnyrr_y069WuuH5ug130_provenance.