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- NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion type Assertion NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_head.
- NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_provenance.
- NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion evidence source_evidence_literature NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_provenance.
- NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion SIO_000772 24236044 NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_provenance.
- NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion wasDerivedFrom befree-20150227 NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_provenance.
- NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion wasGeneratedBy ECO_0000203 NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_provenance.