Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_assertion description "[Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_assertion evidence source_evidence_literature NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_assertion SIO_000772 10762541 NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_assertion wasDerivedFrom befree-2016 NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_assertion wasGeneratedBy ECO_0000203 NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.
- befree-2016 importedOn "2016-02-19" NP280907.RARlpGAXlt1W2XcX4alofo38EZEh_MqLxCV32maaFUuho130_provenance.