Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_assertion description "[study tested for the association of four SNPs of NPTX2 & haplotypes consisting of the SNPs with autism, between autistic patients & controls in a Japanese population; no significant difference was observed in allele, genotype or haplotype frequencies]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_assertion evidence source_evidence_literature NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_assertion SIO_000772 17408830 NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_assertion wasDerivedFrom lhgdn-20090331 NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_assertion wasGeneratedBy ECO_0000203 NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP197808.RAeQxKIayVTc-B68SKT2BGLK8MyXfg-0FhIs25Uva9AiQ130_provenance.