Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_assertion wasGeneratedBy ECO_0000203 NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_assertion wasDerivedFrom befree-20140225 NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_assertion SIO_000772 22236427 NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_assertion evidence source_evidence_literature NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_assertion description "[The discovery that loss-of-function mutations in the gene DOCK8 are responsible for most forms of autosomal recessive hyper-IgE syndrome and some forms of combined immunodeficiency without elevated serum IgE has led to studies into the immunopathogenesis of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.
- befree-20140225 importedOn "2014-02-25" NP623801.RA8YazNqg8TDJG8I5sngwLPpAQ_Aho6UJ5V090wb8Pd00130_provenance.