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- source_evidence_literature type ECO_0000212 NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_assertion description "[The frequency of patients carrying both the TBXA2R+795T>C rare allele and HLA DPB1(*)0301 was significantly higher in AIA patients (29.4%) than in ATA patients (7.3%) (P=0.008, odds ratio=5.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_assertion evidence source_evidence_literature NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_assertion SIO_000772 15898979 NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_assertion wasDerivedFrom befree-20150227 NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_assertion wasGeneratedBy ECO_0000203 NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP452680.RAZVFDygOUocDYCl_jm30qHo0K2NRF5FxzhiaRN9qv3Jk130_provenance.