Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion type Assertion NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_head.
- NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion description "[In conclusion, although NDI is a rare disease, the findings of mutations scattered over the entire coding region of the AVPR2 gene are a valuable model to determine structure function relationship in G-protein-coupled receptor related diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_provenance.
- NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion evidence source_evidence_literature NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_provenance.
- NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion SIO_000772 17020465 NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_provenance.
- NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion wasDerivedFrom befree-20140225 NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_provenance.
- NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_assertion wasGeneratedBy ECO_0000203 NP252026.RAsArjwS44SoKByZmpyxwZJxw1P40kziF4eXRpSQV-t5Y130_provenance.