Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_assertion> ?p ?o ?g. }
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- NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_assertion type Assertion NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_head.
- NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_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." NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_provenance.
- NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_assertion evidence source_evidence_literature NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_provenance.
- NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_assertion SIO_000772 17020465 NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_provenance.
- NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_assertion wasDerivedFrom befree-20140225 NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_provenance.
- NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_assertion wasGeneratedBy ECO_0000203 NP520959.RA-vGjjM1JqzECo2PtzwYlqlHf4Cfg7Qzllct7M1OBAbA130_provenance.