Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_assertion wasGeneratedBy ECO_0000203 NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_assertion wasDerivedFrom lhgdn-20090331 NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_assertion SIO_000772 15017542 NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_assertion evidence source_evidence_literature NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_assertion description "[insertion/deletion polymorphism may be associated with persistent pulmonary hypertension in newborns with congenital diaphragmatic hernia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP147205.RAfkSTS33fdI6tTd-ptIMp915QxTS8D-ih4ePLIKCW5cE130_provenance.