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- source_evidence_literature type ECO_0000212 NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_assertion description "[Primary HLH includes PRF1, UNC13D, STX11, STXBP2, RAB27A, LYST, SH2D1A and XIAP gene mutations; and secondary HLH is associated with infections, malignancies and autoimmune diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_assertion evidence source_evidence_literature NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_assertion SIO_000772 22672194 NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_assertion wasDerivedFrom befree-20150227 NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_assertion wasGeneratedBy ECO_0000203 NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541840.RAVm81st6jO_d0-Qb3b0HwoKWaG7IMh67Svdtnk3UpeHM130_provenance.