Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_assertion description "[Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_assertion evidence source_evidence_literature NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_assertion SIO_000772 14566651 NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_assertion wasDerivedFrom befree-20140225 NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_assertion wasGeneratedBy ECO_0000203 NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428323.RAayfZ49TC1ny83WS53J7keEpKf7xgB86O84Kr0FBwfTI130_provenance.