Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion> ?p ?o ?g. }
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- NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion type Assertion NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_head.
- NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion description "[The present study has identified NKX2.5 and GATA4 constitutional variants in our CHD cohort, but was unable to replicate the previously published findings of high prevalence of somatically derived sequence mutations in patients with cardiac septal defects using fresh-frozen cardiac tissues rather than formalin-fixed tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_provenance.
- NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion evidence source_evidence_literature NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_provenance.
- NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion SIO_000772 21276881 NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_provenance.
- NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion wasDerivedFrom befree-20140225 NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_provenance.
- NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_assertion wasGeneratedBy ECO_0000203 NP896288.RAAXXJe4gg70kQqdnk3Vc31JmU14neCiEe3BM1FHLI4Bc130_provenance.