Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion> ?p ?o ?g. }
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- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion type Assertion NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_head.
- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion description "[A screen of a pool of 81 healthy, unrelated individuals showed no presence for the homozygous form of this allele, suggesting that NFATC1 is a potential VSD-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_provenance.
- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion evidence source_evidence_literature NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_provenance.
- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion SIO_000772 17110989 NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_provenance.
- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion wasDerivedFrom befree-20140225 NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_provenance.
- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion wasGeneratedBy ECO_0000203 NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_provenance.