Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion> ?p ?o ?g. }
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- NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion type Assertion NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_head.
- NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion description "[Mutations of PTPN11, KRAS and SOS1 in the RAS-MAPK pathway cause approximately 60% of cases of Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_provenance.
- NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion evidence source_evidence_literature NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_provenance.
- NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion SIO_000772 17603482 NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_provenance.
- NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion wasDerivedFrom befree-2016 NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_provenance.
- NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_assertion wasGeneratedBy ECO_0000203 NP617880.RAXcYnL0YRsBV5gh5MKa_P9W18e44RzulWEN369DhAkyQ130_provenance.