Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- befree-2016 importedOn "2016-02-19" NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_assertion wasGeneratedBy ECO_0000203 NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_assertion wasDerivedFrom befree-2016 NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_assertion SIO_000772 11968081 NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_assertion evidence source_evidence_literature NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.
- NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_assertion description "[Mutations in RPGR, retinitis pigmentosa GTPase regulator, are associated with RP3 type of X-linked retinitis pigmentosa, a severe, non-syndromic form of retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352745.RAAI744tGkWt_GNRCV1e5ol0psPRBHXE_ZiciwNyZ8Lxs130_provenance.