Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion> ?p ?o ?g. }
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- NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion type Assertion NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_head.
- NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion description "[Although ranked among the least common congenital heart defects, TA provides an excellent model for the role of individual genes in cardiac morphogenesis as exemplified by TBX1 deficiency caused by point mutations or, more commonly, hemizygosity as part of the 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_provenance.
- NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion evidence source_evidence_literature NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_provenance.
- NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion SIO_000772 25713110 NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_provenance.
- NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion wasDerivedFrom befree-2016 NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_provenance.
- NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_assertion wasGeneratedBy ECO_0000203 NP1266165.RAydBZPGbIVywK-LFxK2l8Z3B3NFfez809dXYj_h_ntZk130_provenance.