Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_assertion description "[The results from genetic typing in this study would be useful, in conjunction with results from autoantibody analysis that are prospectively being followed-up in all the babies, to develop an approach for identifying children at risk for developing T1DM. ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_assertion evidence source_evidence_literature NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_assertion SIO_000772 15699508 NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_assertion wasDerivedFrom gad-20150221 NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_assertion wasGeneratedBy ECO_0000203 NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP73946.RA5CBlTtg9rvj9atVWLmCt2shWdIEbx0VgpKnY74TmfnU130_provenance.