Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP892805.RAktw4EViSv-CjGKQV3l0OkCBvuafC4KpkWTkjNWkp1cI130_provenance.