Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_assertion description "[The prevalence of the homozygous CD14 C-260TT genotype was significantly (P = 0.0081) lower in children with T1DM but not in those with CD and T1DM, compared with control children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_assertion evidence source_evidence_literature NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_assertion SIO_000772 18728522 NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_assertion wasDerivedFrom befree-2016 NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_assertion wasGeneratedBy ECO_0000203 NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP689794.RArPdlxWI--HS27JDbz4xM6zm2HFO42Q_QM8PwpRNI_dQ130_provenance.