Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_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." NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_assertion evidence source_evidence_literature NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_assertion SIO_000772 19571582 NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_assertion wasDerivedFrom befree-2016 NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_assertion wasGeneratedBy ECO_0000203 NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.
- befree-2016 importedOn "2016-02-19" NP748770.RAbT-bz5wCHjmFvFkM08ImMgka2C_LRB7lRA8vuibGvDI130_provenance.