Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_assertion description "[Although clinical features associated with the T666M CACNA1A mutation are highly variable, downbeat positioning nystagmus may be an important clinical feature of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_assertion evidence source_evidence_literature NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_assertion SIO_000772 18670797 NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_assertion wasDerivedFrom befree-2016 NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_assertion wasGeneratedBy ECO_0000203 NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.
- befree-2016 importedOn "2016-02-19" NP685395.RAcoB_hOiB9Kt2HApt_lUuDnJqLzlD48yx9EmaWBo5NOY130_provenance.