Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_assertion description "[Compromised function in the Na(v)1.2 Dravet syndrome mutation R1312T.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_assertion evidence source_evidence_literature NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_assertion SIO_000772 22677033 NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_assertion wasDerivedFrom befree-2016 NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_assertion wasGeneratedBy ECO_0000203 NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.
- befree-2016 importedOn "2016-02-19" NP988062.RAGqgmCMRkbC998HcD_qY8aPItZl-ljgWWQVZsF-ca9LY130_provenance.