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- source_evidence_literature type ECO_0000212 NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_assertion description "[Existence of a discrete new X-linked intellectual disability (XLID) syndrome due to KIAA2022 deficiency was questioned by disruption of KIAA2022 by an X-chromosome pericentric inversion in a XLID family we reported in 2004.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_assertion evidence source_evidence_literature NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_assertion SIO_000772 23615299 NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_assertion wasDerivedFrom befree-2016 NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_assertion wasGeneratedBy ECO_0000203 NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1072021.RAmPBB8_2HxDjtRS_h4B9-v_21150b7J3NwY6Qz0xHBXc130_provenance.