Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion type Assertion NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_head.
- NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion description "[We have identified mutations in an X chromosome-linked, Aristaless-related, homeobox gene (ARX), in nine families with mental retardation (syndromic and nonspecific), various forms of epilepsy, including infantile spasms and myoclonic seizures, and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_provenance.
- NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion evidence source_evidence_literature NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_provenance.
- NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion SIO_000772 11889467 NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_provenance.
- NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion wasDerivedFrom befree-20140225 NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_provenance.
- NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_assertion wasGeneratedBy ECO_0000203 NP225253.RAMZ_h_L-L_VXVQSI-fvh8GWp478GfABZD6YX1Zc6UnC4130_provenance.