Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion type Assertion NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_head.
- NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion description "[Fifty-nine percent of childhood-onset patients with T1DM were identified with high genetic risk based on known HLA-DQA1/B1 associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_provenance.
- NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion evidence source_evidence_literature NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_provenance.
- NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion SIO_000772 21418452 NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_provenance.
- NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion wasDerivedFrom befree-20150227 NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_provenance.
- NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_assertion wasGeneratedBy ECO_0000203 NP1015106.RAQ7U83IZs3_ROlEA9xL4S7RRX_7A6iSOdQ1fCQlDytfI130_provenance.