Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_assertion description "[identified 10 mutations in the SCN9A gene encoding the sodium channel protein Nav1.7 in congenital indifference to pain ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_assertion evidence source_evidence_literature NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_assertion SIO_000772 17470132 NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_assertion wasDerivedFrom lhgdn-20090331 NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_assertion wasGeneratedBy ECO_0000203 NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP153772.RAaG8dR3K_VlgC_CvbZX0L89uZgE1X3aiQD4jxRXfoFpU130_provenance.