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- source_evidence_literature type ECO_0000212 NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP835531.RAUVXQ3Ni3J0K5t184RajsjhOppr7aFbS7W-2fVp1UnpQ130_provenance.