Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion> ?p ?o ?g. }
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- NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion type Assertion NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_head.
- NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion description "[After 2006, germline mutations in the KRAS, SOS1, and RAF1 genes were reported to cause Noonan syndrome (NS), in addition to the PTPN11 gene, and now we can find the etiology of disease in approximately 60-70% of NS cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_provenance.
- NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion evidence source_evidence_literature NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_provenance.
- NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion SIO_000772 19020799 NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_provenance.
- NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion wasDerivedFrom gad-20130706 NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_provenance.
- NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_assertion wasGeneratedBy ECO_0000203 NP82210.RAQzDous3dEaSmSIl_kMLwcKzhBHX_DUGtfdXPHVa6yd0130_provenance.