Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_assertion description "[WHIM(warts, hypogammaglobulinemia, recurrent bacterial infection, and myelokathexis) syndrome is a rare immunodeficiency caused in many cases by autosomal dominant C-terminal truncation mutations in the chemokine receptor CXCR4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_assertion evidence source_evidence_literature NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_assertion SIO_000772 16946301 NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_assertion wasDerivedFrom befree-20140225 NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_assertion wasGeneratedBy ECO_0000203 NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP502890.RAmVIxBflSmzYVc_dkeAz_C96cRwXtwPtv4yP88Dd-wmQ130_provenance.