Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_assertion wasGeneratedBy ECO_0000203 NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_assertion wasDerivedFrom befree-20140225 NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_assertion SIO_000772 8037181 NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_assertion evidence source_evidence_literature NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_assertion description "[We have previously reported the absence of mutations within exons 5-9 of the p53 gene in a panel of 30 cases of acute promyelocytic leukemia (APL), which represent the M3 FAB type of acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP409709.RAwdzFfZ2p72yV5p-qTNGrQ_5X8O8onv0O4RDAcpL8Fhg130_provenance.