Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_assertion type Assertion NP286693.RAhn7jMVKS_BIcZCToLMh4Yx0iAF7LCOwQdOVi__N0WXw130_head.
- 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.