Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_assertion description "[A trend towards a reduction of the risk of CD (p = 0.055, OR: 0.22, CI 0.05: 1.04) was observed in patients with T1DM (28% vs T1DM + CD 2%) who did not carry either the HLA-DQA1*0501-DQB1*0201 or the DQA1*0301-DQB1*0302 haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_assertion evidence source_evidence_literature NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_assertion SIO_000772 15174785 NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_assertion wasDerivedFrom befree-2016 NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_assertion wasGeneratedBy ECO_0000203 NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.
- befree-2016 importedOn "2016-02-19" NP446514.RAY73Bhu1tKy7r4aBhWZPzxek60rwE-4bssU3HL2SQxHI130_provenance.