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- source_evidence_literature type ECO_0000212 NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- befree-2016 importedOn "2016-02-19" NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_assertion wasGeneratedBy ECO_0000203 NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_assertion wasDerivedFrom befree-2016 NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_assertion SIO_000772 20663923 NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_assertion evidence source_evidence_literature NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.
- NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_assertion description "[To identify common risk variation, the Autism Genome Project (AGP) Consortium genotyped 1558 rigorously defined ASD families for 1 million single-nucleotide polymorphisms (SNPs) and analyzed these SNP genotypes for association with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828854.RA7t7k-Zb-1IY5Ybbgn2r6o5pJcp2C-wzBQ0np6w6osM0130_provenance.