Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion> ?p ?o ?g. }
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- NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion type Assertion NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_head.
- NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion description "[Disorders caused by mutations in the ARX gene include: hydrocephaly, lissencephaly and agenesis of corpus callosum with abnormal genitalia, Partington syndrome S), X-linked infantile spasms, myoclonic epilepsy, and nonspecific mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_provenance.
- NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion evidence source_evidence_literature NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_provenance.
- NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion SIO_000772 18975239 NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_provenance.
- NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion wasDerivedFrom lhgdn-20090331 NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_provenance.
- NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_assertion wasGeneratedBy ECO_0000203 NP243309.RADnu7b9HACtZ6y1nckksqjtTYC0w4p5Px25peRx4y0p8130_provenance.