Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_assertion> ?p ?o ?g. }
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- NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_assertion type Assertion NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_head.
- NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_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." NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_provenance.
- NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_assertion evidence source_evidence_literature NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_provenance.
- NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_assertion SIO_000772 16235064 NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_provenance.
- NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_assertion wasDerivedFrom befree-20140225 NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_provenance.
- NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_assertion wasGeneratedBy ECO_0000203 NP487848.RAjAbvSwHtJ4gvO6frW2_iCIt8jqatTydPvp41NNkWJPg130_provenance.