Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion> ?p ?o ?g. }
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- NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion type Assertion NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_head.
- NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion description "[Genetic variants have been implicated, including CRELD1 mutations, but no previous study has examined the candidate genes, NKX2-5 and GATA4, in DS patients with secundum atrial defects (ASDII) and ventricular septal defects (VSD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_provenance.
- NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion evidence source_evidence_literature NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_provenance.
- NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion SIO_000772 25524324 NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_provenance.
- NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion wasDerivedFrom befree-2016 NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_provenance.
- NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_assertion wasGeneratedBy ECO_0000203 NP1249430.RAjkaxZPvnYqYJ3gwqzaM_O27EAz92LYxBAvUMpmXntqM130_provenance.