Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_assertion description "[Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_assertion evidence source_evidence_literature NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_assertion SIO_000772 23653000 NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_assertion wasDerivedFrom befree-20150227 NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_assertion wasGeneratedBy ECO_0000203 NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP750464.RAiTJExg4dpMd0NV2ipFgfsAs3fkIggRs1P4kptCQtIgs130_provenance.