Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion evidence source_evidence_literature NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion SIO_000772 17376794 NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion wasDerivedFrom gad-20150221 NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion wasGeneratedBy ECO_0000203 NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.