Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_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." NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_assertion evidence source_evidence_literature NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_assertion SIO_000772 2278970 NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_assertion wasDerivedFrom befree-2016 NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_assertion wasGeneratedBy ECO_0000203 NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.
- befree-2016 importedOn "2016-02-19" NP996907.RAf9O3BtA_9yksmDzzrc-RXE7dn2PNbiyA_Gu9szNvLtg130_provenance.