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- source_evidence_literature type ECO_0000212 NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_assertion description "[MECP2 mutations have also been identified in individuals with a variety of clinical syndromes, including mild learning-disability in females, neonatal encephalopathy in males, and psychiatric disorders, autism and X-linked mental retardation in both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_assertion evidence source_evidence_literature NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_assertion SIO_000772 16647848 NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_assertion wasDerivedFrom befree-20140225 NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_assertion wasGeneratedBy ECO_0000203 NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP829132.RADZS_XE7Z-cOABUhIkp6bkEjnzujnyHAhNWTHTI0BNjY130_provenance.