Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion> ?p ?o ?g. }
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- NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion type Assertion NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_head.
- NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion description "[Mutations in the Aristaless related homeobox (ARX) gene are associated with a broad spectrum of disorders, including nonsyndromic X-linked mental retardation, sometimes associated with epilepsy, as well as syndromic forms with brain abnormalities and abnormal genitalia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_provenance.
- NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion evidence source_evidence_literature NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_provenance.
- NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion SIO_000772 17044103 NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_provenance.
- NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion wasDerivedFrom befree-20140225 NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_provenance.
- NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_assertion wasGeneratedBy ECO_0000203 NP276953.RASXfhDOlCFeLG8GR-cIYBZGnfY4T-qSfpDEcymq4y6lo130_provenance.