Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_assertion description "[We investigated the (CAG)n repeat length of the SCA2 gene in 842 patients with sporadic ataxia and in 96 German families with dominantly inherited SCA which do not harbor the SCA1 or MJD1/SCA3 mutation, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_assertion evidence source_evidence_literature NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_assertion SIO_000772 10735276 NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_assertion wasDerivedFrom befree-2016 NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_assertion wasGeneratedBy ECO_0000203 NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.
- befree-2016 importedOn "2016-02-19" NP279083.RArxgiB9c0dUPggc4HwYdWKuyFPCbmSYFYRYGSM8pjqgw130_provenance.