Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion> ?p ?o ?g. }
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- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion type Assertion NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_head.
- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_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." NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_provenance.
- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion evidence source_evidence_literature NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_provenance.
- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion SIO_000772 22949144 NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_provenance.
- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion wasDerivedFrom befree-20140225 NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_provenance.
- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion wasGeneratedBy ECO_0000203 NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_provenance.