Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion> ?p ?o ?g. }
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- NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion type Assertion NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_head.
- NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_provenance.
- NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion evidence source_evidence_literature NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_provenance.
- NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion SIO_000772 16235064 NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_provenance.
- NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion wasDerivedFrom befree-2016 NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_provenance.
- NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_assertion wasGeneratedBy ECO_0000203 NP518622.RAQzY3cb7GXQwhvLqn1jwsZugAun5Fcue34Ayi2yPEfog130_provenance.