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- source_evidence_literature type ECO_0000212 NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion wasGeneratedBy ECO_0000203 NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion wasDerivedFrom befree-20150227 NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion SIO_000772 17319270 NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion evidence source_evidence_literature NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.
- NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion description "[CBS gene G919A mutation is associated with the development of CHD, and the mutated allele may decrease the risk of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_provenance.