Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_assertion description "[In addition to the juxtacentromeric heterochromatic instability, the disease is characterized by variable reduction in serum immunoglobulin levels which cause most ICF patients to succumb to infectious diseases before adulthood as well as exhibit facial dysmorphism including hypertelorism, epicanthal folds, and low-set ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_assertion evidence source_evidence_literature NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_assertion SIO_000772 21120685 NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_assertion wasDerivedFrom befree-20140225 NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_assertion wasGeneratedBy ECO_0000203 NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.