Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion> ?p ?o ?g. }
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- NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion type Assertion NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_head.
- NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion description "[We tested genomic deoxyribonucleic acid from 608 prospectively recruited patients with conotruncal anomalies (n = 370), left-sided lesions (n = 160), secundum atrial septal defect (ASD) (n = 71), and Ebstein's malformation (n = 7) for NKX2.5 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_provenance.
- NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion evidence source_evidence_literature NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_provenance.
- NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion SIO_000772 14607454 NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_provenance.
- NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion wasDerivedFrom befree-2016 NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_provenance.
- NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_assertion wasGeneratedBy ECO_0000203 NP419888.RAh6qfYbiu3lyCirtRixqy0SCmIOsmKTP3r1vYWCqWL_s130_provenance.