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- source_evidence_literature type ECO_0000212 NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_assertion description "[We incorporated data from HLA typing (HLA-A, -B, -C, -DRB3, -DRB1, -DQB1) and single nucleotide polymorphisms across the MHC (n?=?18,644; genotyped and imputed) alongside previously suggested PSC risk determinants in the MHC, i.e. amino acid variation of DR?, a MICA microsatellite polymorphism and HLA-C and HLA-B according to their ligand properties for killer immunoglobulin-like receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_assertion evidence source_evidence_literature NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_assertion SIO_000772 25521205 NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_assertion wasDerivedFrom befree-2016 NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_assertion wasGeneratedBy ECO_0000203 NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249153.RA7dqT0FiubsOQP6HB8m1nPU6WAhR1DIvXqcZYMUodCrk130_provenance.