Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_assertion description "[We conclude that EFMR is a distinctive, under-recognized familial syndrome where girls present with convulsions in infancy, often associated with intellectual impairment and autistic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_assertion evidence source_evidence_literature NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_assertion SIO_000772 18234694 NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_assertion wasDerivedFrom befree-20140225 NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_assertion wasGeneratedBy ECO_0000203 NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718715.RAmLIrlwpeMiZrK462NL2SV2PNCc8M_0W4ab0q1h_PyOk130_provenance.