Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_assertion description "[We also genotyped the UC-associated ECM1 variant rs11205387 in 1560 CD patients and 3028 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_assertion evidence source_evidence_literature NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_assertion SIO_000772 19068216 NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_assertion wasDerivedFrom befree-20150227 NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_assertion wasGeneratedBy ECO_0000203 NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP364145.RAhrFZLqzRdDuwlK4qgaumkd8RzyLsuG_9Gv-pbFOK8qQ130_provenance.