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- source_evidence_literature type ECO_0000212 NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_assertion wasGeneratedBy ECO_0000203 NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_assertion wasDerivedFrom befree-20140225 NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_assertion SIO_000772 17847002 NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_assertion evidence source_evidence_literature NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_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." NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP268160.RAXInF6uVQfTJUZgeXWy4bD3jO7tF0kpp4LF-g4vc3JRQ130_provenance.