Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_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." NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_assertion evidence source_evidence_literature NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_assertion SIO_000772 21857984 NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_assertion wasDerivedFrom befree-20140225 NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_assertion wasGeneratedBy ECO_0000203 NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP654398.RAUa9hVcCpkSGn80nFXdOPcI4W4u_ehb-PU9VME2v17xM130_provenance.