Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_assertion> ?p ?o ?g. }
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- NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_assertion type Assertion NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_head.
- NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_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." NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_provenance.
- NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_assertion evidence source_evidence_literature NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_provenance.
- NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_assertion SIO_000772 19020799 NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_provenance.
- NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_assertion wasDerivedFrom gad-20130706 NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_provenance.
- NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_assertion wasGeneratedBy ECO_0000203 NP71089.RA5aqnzirtRqzG3J6JFnEAeavEikWs9A0Iqy_Fz_33pM4130_provenance.