Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_assertion wasGeneratedBy ECO_0000203 NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_assertion wasDerivedFrom befree-20150227 NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_assertion SIO_000772 1363103 NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_assertion evidence source_evidence_literature NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.
- NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_assertion description "[All the immune-deficient patients in this family possessed at least one copy of an MHC haplotype previously shown to be abnormally frequent in IgA-D and CVID: HLA-DQB1*0201, HLA-DR3, C4B-Sf, C4A-deleted, G11-15, Bf-0.4, C2-a, HSP70-7.5, TNF alpha-5, HLA-B8, and HLA-A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454099.RACMbnEXyFq6RZaFz0csaLWe6IvzH4MYgE4rmOXg11SpI130_provenance.