Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_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." NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_assertion evidence source_evidence_literature NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_assertion SIO_000772 18258668 NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_assertion wasDerivedFrom befree-20140225 NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_assertion wasGeneratedBy ECO_0000203 NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP513019.RAcHn1M8hf1PghlzOpO_haWdaTzo57whHsdThP3jEXR7I130_provenance.