Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_assertion wasGeneratedBy ECO_0000203 NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_assertion wasDerivedFrom befree-20150227 NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_assertion SIO_000772 21094958 NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_assertion evidence source_evidence_literature NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.
- NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_assertion description "[Gain-of-function mutations in the SCN9A gene (encoding to NaV1.7 voltage-gated sodium channel) cause two rare paroxysmal pain disorders: inherited erythromelalgia (IEM) and paroxysmal extreme pain disorder (PEDP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683520.RANAskLUqSgruzToZD3oNn0wJD4TkFrtk3eaVue_sX8hI130_provenance.