Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion> ?p ?o ?g. }
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- NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion type Assertion NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_head.
- NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion wasGeneratedBy ECO_0000203 NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_provenance.
- NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion wasDerivedFrom befree-20140225 NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_provenance.
- NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion SIO_000772 17847002 NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_provenance.
- NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion evidence source_evidence_literature NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_provenance.
- NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_assertion description "[This extensive study, involving multiple independent populations, provides the first evidence that genetic variants in LRP8 may contribute to the development of premature and familial CAD and MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781500.RAO1R7d4RLXtMnGqtf9ghNXyvIs20gvUfk6aae50S1JTI130_provenance.