Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_assertion wasGeneratedBy ECO_0000203 NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_assertion wasDerivedFrom befree-20140225 NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_assertion SIO_000772 16272056 NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_assertion evidence source_evidence_literature NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_assertion description "[Aiming towards an understanding of the molecular background of retinitis pigmentosa, this paper describes the phenotype of a Swedish family with a mutation in IMPDH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859657.RA6k7vTku3-aaxdQL17a3OAx2aNFVdhlfy9hZ9q6FZVH4130_provenance.