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- source_evidence_literature type ECO_0000212 NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_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." NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_assertion evidence source_evidence_literature NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_assertion SIO_000772 20517688 NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_assertion wasDerivedFrom befree-2016 NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_assertion wasGeneratedBy ECO_0000203 NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
- befree-2016 importedOn "2016-02-19" NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.