Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_assertion description "[X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_assertion evidence source_evidence_literature NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_assertion SIO_000772 18469813 NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_assertion wasDerivedFrom befree-20140225 NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_assertion wasGeneratedBy ECO_0000203 NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP525905.RAHQ0x96LAwxIPIFuC-LALXBxiIspyoFGSt-TnzQvMD8o130_provenance.