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- source_evidence_literature type ECO_0000212 NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_assertion description "[No associations were found between IL1B C(-31)T or IL1RN VNTR genotypes, alleles or haplotypes and the severity of CAD when subgroups with SVD and MVD were compared.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_assertion evidence source_evidence_literature NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_assertion SIO_000772 21840356 NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_assertion wasDerivedFrom befree-20140225 NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_assertion wasGeneratedBy ECO_0000203 NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_provenance.