Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_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." NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_assertion evidence source_evidence_literature NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_assertion SIO_000772 23615299 NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_assertion wasDerivedFrom befree-20140225 NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_assertion wasGeneratedBy ECO_0000203 NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870647.RAGWsvqZ-ebX0RehCpVdbdGBD5XKScQcRlQlEIgsn1fnk130_provenance.