Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_assertion description "[In addition, specific HNF4A genetic variants have been identified in pediatric cohorts of Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_assertion evidence source_evidence_literature NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_assertion SIO_000772 24415854 NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_assertion wasDerivedFrom befree-2016 NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_assertion wasGeneratedBy ECO_0000203 NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1144311.RA_OZLpD_2S84NMm_4wZA8s-JvvkHiP_eoxGV3vhECwuQ130_provenance.