about
SNPPhenA: a corpus for extracting ranked associations of single-nucleotide polymorphisms and phenotypes from literaturenala: text mining natural language mutation mentions.tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.The SNPcurator: literature mining of enriched SNP-disease associations.LitVar: a semantic search engine for linking genomic variant data in PubMed and PMC.DES-Mutation: System for Exploring Links of Mutations and Diseases
P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
SETH detects and normalizes genetic variants in text.
@en
SETH detects and normalizes genetic variants in text.
@nl
type
label
SETH detects and normalizes genetic variants in text.
@en
SETH detects and normalizes genetic variants in text.
@nl
prefLabel
SETH detects and normalizes genetic variants in text.
@en
SETH detects and normalizes genetic variants in text.
@nl
P2093
P2860
P356
P1433
P1476
SETH detects and normalizes genetic variants in text.
@en
P2093
Jörg Hakenberg
Philippe Thomas
Tim Rocktäschel
Yvonne Lichtblau
P2860
P304
P356
10.1093/BIOINFORMATICS/BTW234
P407
P577
2016-06-02T00:00:00Z