Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_assertion description "[Common genetic variants in four genes (GREM1, EYA1, ROBO2 and UPK3A) show a trend towards association with the development of primary VUR (GREM1, EYA1, ROBO2) or duplex collecting system (EYA1 and UPK3A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_assertion evidence source_evidence_literature NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_assertion SIO_000772 22558067 NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_assertion wasDerivedFrom befree-20150227 NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_assertion wasGeneratedBy ECO_0000203 NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP767121.RA7Qkinj-iLeaZj-LeSaADqoB5EMGrvbaEVlatReYq9tM130_provenance.