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- source_evidence_literature type ECO_0000212 NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_assertion description "[Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_assertion evidence source_evidence_literature NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_assertion SIO_000772 21359847 NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_assertion wasDerivedFrom befree-20140225 NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_assertion wasGeneratedBy ECO_0000203 NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP905733.RAMMzF5Zg2oGbEa5cAlLKX1UD_v1HOAu249SEGwqsnKEU130_provenance.