Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_assertion description "[We report on the evaluation of a strategy for screening for XNP/ATR-X mutations in males with mental retardation and associated dysmorphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_assertion evidence source_evidence_literature NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_assertion SIO_000772 10204841 NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_assertion wasDerivedFrom befree-20140225 NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_assertion wasGeneratedBy ECO_0000203 NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP538357.RARxCtYbFSswwis8buDQgTKtGLfFhNnnHHU0Ae0eIWLvU130_provenance.