Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_assertion> ?p ?o ?g. }
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- NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_assertion type Assertion NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_head.
- NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_assertion wasGeneratedBy ECO_0000203 NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_provenance.
- NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_assertion wasDerivedFrom lhgdn-20090331 NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_provenance.
- NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_assertion SIO_000772 15017542 NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_provenance.
- NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_assertion evidence source_evidence_literature NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_provenance.
- NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_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." NP203510.RAbImtrwsqplwNy9sXsIJTp5DXJriTUNcHtt55tsPf7Mg130_provenance.