Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_assertion description "[Autosomal dominant gain-of-function truncations of CXCR4 are associated with warts, hypo-gammaglobulinemia, infections, and myelokathexis (WHIM) syndrome, a primary immunodeficiency disorder characterized by neutropenia and recurrent infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_assertion evidence source_evidence_literature NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_assertion SIO_000772 20592249 NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_assertion wasDerivedFrom befree-2016 NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_assertion wasGeneratedBy ECO_0000203 NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.
- befree-2016 importedOn "2016-02-19" NP822691.RAo0fQj7iEqHD4qhw5KYM8mLKvbFcsdRB5jgtzOIUVlBs130_provenance.