Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- befree-2016 importedOn "2016-02-19" NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_assertion wasGeneratedBy ECO_0000203 NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_assertion wasDerivedFrom befree-2016 NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_assertion SIO_000772 15017542 NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_assertion evidence source_evidence_literature NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.
- NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_assertion description "[These data suggest that D allele of the ACE gene insertion/deletion polymorphism and angiotensinogen M235 T polymorphism may be associated with PPH in newborns with congenital diaphragmatic hernia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435458.RAiGYVE8oo5ghX9U74veuFfq-u3aSSNw3igtu8sqbEYFc130_provenance.