Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_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." NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion evidence source_evidence_literature NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion SIO_000772 16647848 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion wasDerivedFrom befree-20140225 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion wasGeneratedBy ECO_0000203 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.