Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_assertion description "[The LQTS is caused by mutations in genes encoding cardiac ion channels, and mutations in the genes KVLQT1 and SCNA5 have been identified in cases initially diagnosed as SIDS, in addition to several polymorphisms in these 2 genes and in the HERG gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_assertion evidence source_evidence_literature NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_assertion SIO_000772 15466077 NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_assertion wasDerivedFrom befree-20150227 NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_assertion wasGeneratedBy ECO_0000203 NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP523195.RA0YNGvCp4Ktc5a_qmgXo2IKxjqfXn0IhyYOWF7yU4QBU130_provenance.