Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_assertion description "[High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_assertion evidence source_evidence_literature NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_assertion SIO_000772 11595021 NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_assertion wasDerivedFrom gad-20150221 NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_assertion wasGeneratedBy ECO_0000203 NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP71623.RATprjoC3GLTaBW13UNKTJJsQIdHXZbJ-H5F7MyRfgQyI130_provenance.