Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_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." NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_assertion evidence source_evidence_literature NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_assertion SIO_000772 23615299 NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_assertion wasDerivedFrom befree-20150227 NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_assertion wasGeneratedBy ECO_0000203 NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP985846.RAB2QYGKTGZIqi5kXsxsR4NC867D0Ox3JtC5j3Q6MxPzE130_provenance.