Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion description "[Mutations at codon 12, 13, and 61 of the HRAS, KRAS, and NRAS genes were evaluated in 99 cases of pediatric acute myeloid leukemia (AML) using oligonucleotide hybridization to polymerase chain reacted derived products.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion evidence source_evidence_literature NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion SIO_000772 2278970 NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion wasDerivedFrom befree-20140225 NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion wasGeneratedBy ECO_0000203 NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance.