Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion description "[The present findings, together with a previous negative study on MAPT and SOD1 mutation, further elucidated the lack of causative mutations in all exons, exon-intron boundaries, or some rearrangements of the reported major causative or susceptible genes related to ALS, FTLD, parkinsonism, synucleinopathy, TDP-43 proteinopathy, and tauopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion evidence source_evidence_literature NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion SIO_000772 18759352 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion wasDerivedFrom befree-2016 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_assertion wasGeneratedBy ECO_0000203 NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.
- befree-2016 importedOn "2016-02-19" NP690756.RABix091wlDnB_0KLBEYy-eLz2S4bSVWg_tWGrwvvt6VY130_provenance.