Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_assertion description "[The insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE-ins/del) and the angiotensin II type 1 receptor 1166A/C polymorphism (ATR1166A/C) were reported to be associated with several unfavorable outcome parameters in preterm infants like bronchopulmonary dysplasia, persistent ductus arteriosus and impaired insulin sensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_assertion evidence source_evidence_literature NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_assertion SIO_000772 19571582 NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_assertion wasDerivedFrom befree-20140225 NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_assertion wasGeneratedBy ECO_0000203 NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP528637.RASLSM7bllo6cUI9pP_vFzmRVIyQSEK5cpueXofVQ6ZKs130_provenance.