Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_assertion wasGeneratedBy ECO_0000203 NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_assertion wasDerivedFrom befree-20140225 NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_assertion SIO_000772 1363103 NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_assertion evidence source_evidence_literature NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_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." NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551476.RAxgNEuMff-UFI67b_k9yaB_fdZAZX99RQVijZujR1LZU130_provenance.