Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_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." NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_assertion evidence source_evidence_literature NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_assertion SIO_000772 18258668 NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_assertion wasDerivedFrom befree-2016 NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_assertion wasGeneratedBy ECO_0000203 NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.
- befree-2016 importedOn "2016-02-19" NP654355.RAhGrPgt8R1iHsbKIvUBQoCWQMDtGPzX4otVZiD7XvQHc130_provenance.