Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_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." NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_assertion evidence source_evidence_literature NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_assertion SIO_000772 2278970 NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_assertion wasDerivedFrom befree-20140225 NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_assertion wasGeneratedBy ECO_0000203 NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP751310.RAx--x6wwsdC8H1tv1QrcuCKZRRb1M0syqLXH6t1HggYA130_provenance.