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- source_evidence_literature type ECO_0000212 NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_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." NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_assertion evidence source_evidence_literature NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_assertion SIO_000772 20517688 NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_assertion wasDerivedFrom befree-2016 NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_assertion wasGeneratedBy ECO_0000203 NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
- befree-2016 importedOn "2016-02-19" NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.