Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_assertion description "[All mutations of atlastin1 in young-onset autosomal dominant spastic paraplegia patients in France were found in exons 7, 8, 12, and 13/exons should be given priority when performing molecular diagnoses for SPG3A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_assertion evidence source_evidence_literature NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_assertion SIO_000772 15596607 NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_assertion wasDerivedFrom lhgdn-20090331 NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_assertion wasGeneratedBy ECO_0000203 NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP208244.RAiplXr4NFN2GSyHNE3dS8Wh30c1Dy5gGAESKcmO-ZmCo130_provenance.