Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion> ?p ?o ?g. }
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- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion type Assertion NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_head.
- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion description "[Thus, even important for cardiac development, germline mutations in NKX2.5 are rare in patients with sporadic CHD and genetic and/or pathophysiologic heterogeneity is likely for sporadic forms of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_provenance.
- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion evidence source_evidence_literature NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_provenance.
- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion SIO_000772 20456451 NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_provenance.
- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion wasDerivedFrom befree-20150227 NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_provenance.
- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion wasGeneratedBy ECO_0000203 NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_provenance.