Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_assertion> ?p ?o ?g. }
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- NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_assertion type Assertion NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_head.
- NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_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." NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_assertion evidence source_evidence_literature NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_assertion SIO_000772 17020465 NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_assertion wasDerivedFrom befree-20140225 NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_assertion wasGeneratedBy ECO_0000203 NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.