Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_assertion description "[Warts, hypogammaglobulinaemia, infections, myelokathexis (WHIM) syndrome is an inherited immune disorder associated with CXCR4 gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_assertion evidence source_evidence_literature NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_assertion SIO_000772 16899028 NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_assertion wasDerivedFrom befree-20140225 NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_assertion wasGeneratedBy ECO_0000203 NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.