Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_assertion wasGeneratedBy ECO_0000203 NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_assertion wasDerivedFrom befree-20150227 NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_assertion SIO_000772 22304542 NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_assertion evidence source_evidence_literature NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.
- NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_assertion description "[The eNOS 894T allele carriers are at greater risk for both MtS and ED, suggesting that eNOS G894T gene polymorphism might play an implication as a common genetic susceptibility factor to develop both disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP594773.RAOWaxj5oCLoJxY9v_3Wpr4cC9ky47EmzpKfCCINcYqHg130_provenance.