Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion> ?p ?o ?g. }
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- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion type Assertion NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_head.
- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion description "[Mutations in human NKX2.5 cause a variety of cardiac anomalies and may account for a clinically significant portion of tetralogy of Fallot and idiopathic AV block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_provenance.
- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion evidence source_evidence_literature NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_provenance.
- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion SIO_000772 10587520 NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_provenance.
- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion wasDerivedFrom befree-20140225 NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_provenance.
- NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_assertion wasGeneratedBy ECO_0000203 NP274223.RALWUFnRlHlhvIolI_LCbqKXgCrQ3zbtafWenPsoTx3wY130_provenance.