Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_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." NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_assertion evidence source_evidence_literature NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_assertion SIO_000772 19073967 NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_assertion wasDerivedFrom befree-2016 NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_assertion wasGeneratedBy ECO_0000203 NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.
- befree-2016 importedOn "2016-02-19" NP708462.RAFjcIfn5PIW8c9HkYAbEDZUSdKZYR6iJGcWYluiJHKRM130_provenance.