Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_assertion wasGeneratedBy ECO_0000203 NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_assertion wasDerivedFrom befree-2016 NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_assertion SIO_000772 17715352 NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_assertion evidence source_evidence_literature NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.
- NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_assertion description "[A mutation located in exon 10 has been identified in several FTDP-17 families that present with increased exon 10 inclusion in both mRNA and protein, parkinsonism, movement disorders, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626378.RAbXfYrKjAFirU2wak0mSEP6LVmUM1XQaFLsYNYv0muRQ130_provenance.