Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_assertion description "[Oncogenic mutations of gene RAS are most frequent and detected in 20% - 30% of human leukemias and 10% - 15% of MDS cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_assertion evidence source_evidence_literature NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_assertion SIO_000772 19698268 NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_assertion wasDerivedFrom befree-2016 NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_assertion wasGeneratedBy ECO_0000203 NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.
- befree-2016 importedOn "2016-02-19" NP758932.RAukFV1QXU1WhvHkUkg6aZHIKVkVXX0prDzshb4u2l2HE130_provenance.