Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion> ?p ?o ?g. }
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- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion type Assertion NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_head.
- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion wasGeneratedBy ECO_0000203 NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_provenance.
- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion wasDerivedFrom befree-20140225 NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_provenance.
- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion SIO_000772 9243090 NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_provenance.
- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion evidence source_evidence_literature NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_provenance.
- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion description "[Deletions were rare among patients lacking typical DiGeorge syndrome (DGS) or velocardiofacial (VCF) dysmorphic features, and more common in tetralogy of Fallot with pulmonary atresia than tetralogy of Fallot alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_provenance.