Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion type Assertion NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_head.
- 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.