Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion> ?p ?o ?g. }
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- NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion type Assertion NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_head.
- NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion description "[An overview of the association between congenital malformations and VEGF/NOTCH polymorphisms in humans will be discussed along with their potential mechanisms and processes as revealed by transgenic mouse models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_provenance.
- NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion evidence source_evidence_literature NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_provenance.
- NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion SIO_000772 22683047 NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_provenance.
- NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion wasDerivedFrom befree-2016 NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_provenance.
- NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_assertion wasGeneratedBy ECO_0000203 NP988518.RANtmEa79Oj6C7Q8t4OvkVkoBrBvnhhtQl94d4otkmnbY130_provenance.