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- NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_assertion type Assertion NP226940.RAUDEVdMU1b6EDbHlvXcmncoUTBAt2XRboyFAb_7RtHsM130_head.
- 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.