Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_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." NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_assertion evidence source_evidence_literature NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_assertion SIO_000772 19571582 NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_assertion wasDerivedFrom befree-20150227 NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_assertion wasGeneratedBy ECO_0000203 NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP348811.RAy6tNxRo5-Z8pZMkMIx5p1fGLT17ssDNnAnqfPeRoh8A130_provenance.