Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion> ?p ?o ?g. }
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- NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion type Assertion NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_head.
- NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion description "[A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion evidence source_evidence_literature NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion SIO_000772 21426321 NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion wasDerivedFrom befree-20150227 NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_assertion wasGeneratedBy ECO_0000203 NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.