Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_assertion description "[The 32-bp insertion-deletion variant on chromosome 3p21 was newly identified as a type 1 diabetes locus (P=1.81x10(-8)) and was also associated with celiac disease, along with PTPN2 on chromosome 18p11 and CTLA4 on chromosome 2q33, bringing the total number of loci with evidence of a shared association to seven, including SH2B3 on chromosome 12q24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_assertion evidence source_evidence_literature NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_assertion SIO_000772 19073967 NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_assertion wasDerivedFrom gad-20150221 NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_assertion wasGeneratedBy ECO_0000203 NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136430.RAWPpInfMR53R3gBP4MnIiXpRddc7FiMrxGgp5rKKjqxw130_provenance.