Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_assertion description "[Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_assertion evidence source_evidence_literature NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_assertion SIO_000772 17383248 NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_assertion wasDerivedFrom gad-20130706 NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_assertion wasGeneratedBy ECO_0000203 NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64610.RAvJVIed_8zzI6Ln2LBH5kimmHf_kb4x4vUxggzErFCYk130_provenance.