Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_assertion description "[Results of the current study support a causative role for the A1166 C polymorphism of the angiotensin II type 1 gene polymorphism in the pathogenesis or phenotypic expression of polycystic ovary syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_assertion evidence source_evidence_literature NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_assertion SIO_000772 23564192 NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_assertion wasDerivedFrom befree-20140225 NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_assertion wasGeneratedBy ECO_0000203 NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP919118.RAqFIrZRBdPl52Esy7WvvJ8w1-yUMg1IwT7EOhZK7mGRQ130_provenance.