Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion> ?p ?o ?g. }
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- NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion type Assertion NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_head.
- NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion description "[Mutations in the Aristaless-related homeobox gene (ARX) are associated with a wide variety of neurologic disorders including lissencephaly, hydrocephaly, West syndrome, Partington syndrome, and X-linked intellectual disability with or without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_provenance.
- NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion evidence source_evidence_literature NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_provenance.
- NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion SIO_000772 22252899 NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_provenance.
- NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion wasDerivedFrom befree-20140225 NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_provenance.
- NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_assertion wasGeneratedBy ECO_0000203 NP804885.RAy6qr8ET2ij_SY1ogFZdoU4bmiy2w-mlPtwwtNA2oXCs130_provenance.