Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_assertion wasGeneratedBy ECO_0000203 NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_assertion wasDerivedFrom befree-20150227 NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_assertion SIO_000772 16630162 NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_assertion evidence source_evidence_literature NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.
- NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_assertion description "[Machado-Joseph disease [MJD, also spinocerebellar ataxia type 3 (SCA3)] and familial amyloid polyneuropathy type I (FAP-I or ATTR V30M) are neurodegenerative disorders, inherited in an autosomal dominant fashion, which have a high prevalence in Portugal, probably due to a founder effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761641.RAYFykuB3yk0gZx_3fS2itRDqmq8sVb9J_PmnFWyvL7eE130_provenance.