Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_assertion description "[Our study confirms the link between INF2 mutations and CMT-associated glomerulopathy and widens the spectrum of pathogenic mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_assertion evidence source_evidence_literature NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_assertion SIO_000772 22961558 NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_assertion wasDerivedFrom befree-20140225 NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_assertion wasGeneratedBy ECO_0000203 NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP262559.RA_EM9Kx10SNuJRxCn4eqsHN3Hw3VXSxPhKfqXWiezljA130_provenance.