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- source_evidence_literature type ECO_0000212 NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_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." NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_assertion evidence source_evidence_literature NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_assertion SIO_000772 17603482 NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_assertion wasDerivedFrom befree-2016 NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_assertion wasGeneratedBy ECO_0000203 NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.
- befree-2016 importedOn "2016-02-19" NP617875.RAJaN5HAWguNFHhSGr4xzGfEQ_zrs2jnqpYb8Aic_223I130_provenance.