Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion type Assertion NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_head.
- NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_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." NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_provenance.
- NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion evidence source_evidence_literature NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_provenance.
- NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion SIO_000772 20517688 NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_provenance.
- NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion wasDerivedFrom befree-2016 NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_provenance.
- NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion wasGeneratedBy ECO_0000203 NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_provenance.