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- NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_assertion type Assertion NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_head.
- NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_provenance.
- NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_assertion evidence source_evidence_literature NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_provenance.
- NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_assertion SIO_000772 16235064 NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_provenance.
- NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_assertion wasDerivedFrom befree-20150227 NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_provenance.
- NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_assertion wasGeneratedBy ECO_0000203 NP978137.RARs1pjYPuQlJe5_-JleqU7JdXo_DVkf22t2BfyEuU9LM130_provenance.