Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion> ?p ?o ?g. }
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- NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion type Assertion NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_head.
- NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_provenance.
- NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion evidence source_evidence_literature NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_provenance.
- NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion SIO_000772 20738937 NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_provenance.
- NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion wasDerivedFrom gad-20150221 NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_provenance.
- NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_assertion wasGeneratedBy ECO_0000203 NP114804.RAtNsz4MmXaK_g0IaoRXPtvvl2L52zf5tUROERAwtlX2Q130_provenance.