Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion> ?p ?o ?g. }
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- NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion type Assertion NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_head.
- NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion description "[Study reports that 18 of 231 individuals with Noonan syndrome and 2 of 6 individuals with LEOPARD syndrome without PTPN11 mutations have missense mutations in RAF1, which encodes a serine-threonine kinase that activates MEK1 and MEK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_provenance.
- NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion evidence source_evidence_literature NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_provenance.
- NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion SIO_000772 17603483 NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_provenance.
- NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion wasDerivedFrom lhgdn-20090331 NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_provenance.
- NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_assertion wasGeneratedBy ECO_0000203 NP186652.RAPg2Fry5cKTvSc3dvgId49oK5kKORWmGHf_1u42X8yJQ130_provenance.