Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion> ?p ?o ?g. }
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- NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion type Assertion NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_head.
- NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion description "[Aristaless-related homeobox gene (ARX) mutation leads to several neurological disorders including X-linked lissencephaly with abnormal genitalia (XLAG), West syndrome and Partington syndrome, with XLAG being the most severe form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_provenance.
- NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion evidence source_evidence_literature NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_provenance.
- NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion SIO_000772 20538404 NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_provenance.
- NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion wasDerivedFrom befree-20140225 NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_provenance.
- NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_assertion wasGeneratedBy ECO_0000203 NP376798.RAmHesVOBMG3vFqp6HMMUvEutjr5lbiMiUgaXR6TGB4SA130_provenance.