Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion> ?p ?o ?g. }
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- NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion type Assertion NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_head.
- NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion description "[The findings indicate that TGFBR2 gene mutations are responsible for sCAD in 3.6% (95% CI 0.0 to 8.4) of cases, have implications in understanding the role of TGF? signalling in the pathogenesis of sCAD and emphasise the importance of considering molecular characterisation of the TGFBR2 gene in these patients, regardless of the presence of clinical features suggestive of hereditary connective tissue disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_provenance.
- NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion evidence source_evidence_literature NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_provenance.
- NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion SIO_000772 21270064 NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_provenance.
- NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion wasDerivedFrom befree-20150227 NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_provenance.
- NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_assertion wasGeneratedBy ECO_0000203 NP734290.RAZrGOFyxPSnIDrYeP8v_DYAhywEKdbSX8OrXL9j79IrY130_provenance.