Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_assertion> ?p ?o ?g. }
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- NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_assertion type Assertion NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_head.
- NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_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." NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_provenance.
- NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_assertion evidence source_evidence_literature NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_provenance.
- NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_assertion SIO_000772 17603482 NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_provenance.
- NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_assertion wasDerivedFrom befree-2016 NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_provenance.
- NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_assertion wasGeneratedBy ECO_0000203 NP617877.RAe9pBiMEVKvUz6o9BKYvXwIGiqSgeSkc7VPgCraYbSPk130_provenance.