Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_assertion description "[In the present study an FSCN2 mutation was examined that has been reported, not only in patients with retinitis pigmentosa (RP), but also in the normal population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_assertion evidence source_evidence_literature NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_assertion SIO_000772 18450588 NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_assertion wasDerivedFrom befree-20140225 NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_assertion wasGeneratedBy ECO_0000203 NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.
- befree-20140225 importedOn "2014-02-25" NP166088.RALs7n6yyacJR2uS3ls3X232nKBFnybGFHqUQLjtSV3Js130_provenance.