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- source_evidence_literature type ECO_0000212 NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_assertion evidence source_evidence_literature NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_assertion SIO_000772 20517688 NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_assertion wasDerivedFrom befree-20150227 NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_assertion wasGeneratedBy ECO_0000203 NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.