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- source_evidence_literature type ECO_0000212 NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_assertion wasGeneratedBy ECO_0000203 NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_assertion wasDerivedFrom befree-20150227 NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_assertion SIO_000772 17056636 NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_assertion evidence source_evidence_literature NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.
- NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_assertion description "[Remarkably, our cohort of individuals with KRAS mutations showed a high clinical variability, ranging from Noonan syndrome to CFC, and also included two patients who met the clinical criteria of Costello syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527851.RAGrue-Bi3wERYem0dnn7XizdOpejqbUkKGJ_sC4qzM9A130_provenance.