Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_assertion wasGeneratedBy ECO_0000203 NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_assertion wasDerivedFrom befree-2016 NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_assertion SIO_000772 23884151 NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_assertion evidence source_evidence_literature NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.
- NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_assertion description "[Genetic alterations in the SCN1A gene coding for the α-subunit of the neuronal voltage-gated sodium ion channel, type 1 (NaV 1.1), is associated with a spectrum of seizure-related disorders in human, ranging from a relatively milder form of febrile seizures to a more severe epileptic condition known as the Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1096488.RAhRRPnnuM7U4jhttoXNTj64BMbDTz4so1i2ZlzxjsqcE130_provenance.