Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion evidence source_evidence_literature NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion SIO_000772 22949144 NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion wasDerivedFrom befree-2016 NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion wasGeneratedBy ECO_0000203 NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.