Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion> ?p ?o ?g. }
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- NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion type Assertion NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_head.
- NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion wasGeneratedBy ECO_0000203 NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_provenance.
- NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion wasDerivedFrom befree-2016 NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_provenance.
- NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion SIO_000772 10587520 NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_provenance.
- NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion evidence source_evidence_literature NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_provenance.
- NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_assertion description "[The coinheritance of NKX2.5 mutations with various congenital heart defects suggests that this transcription factor contributes to diverse cardiac developmental pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269269.RApDbU_OJ8pAGwaV_dT22irean5CM2OPNPznbzUDdbx48130_provenance.