Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_assertion description "[Hp2-2 was less frequent in patients than in controls (P = 0.0023), but patients having this phenotype were at an increased risk for severe malabsorption (OR 2.21, 95% CI 1.60-3.07) and accounted for 45.3% of all malabsorption cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_assertion evidence source_evidence_literature NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_assertion SIO_000772 18258668 NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_assertion wasDerivedFrom befree-20140225 NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_assertion wasGeneratedBy ECO_0000203 NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP852190.RAFVzLNMc5f2hW6m-98rQCBT4sJZ9RP2D25Tfq3IusTfg130_provenance.