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- source_evidence_literature type ECO_0000212 NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_assertion evidence source_evidence_literature NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_assertion SIO_000772 21264219 NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_assertion wasDerivedFrom befree-2016 NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_assertion wasGeneratedBy ECO_0000203 NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- befree-2016 importedOn "2016-02-19" NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.