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- source_evidence_literature type ECO_0000212 NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_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." NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_assertion evidence source_evidence_literature NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_assertion SIO_000772 20517688 NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_assertion wasDerivedFrom befree-20140225 NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_assertion wasGeneratedBy ECO_0000203 NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.