Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_assertion description "[We highlight the importance of considering the diagnosis of AOA1 in children with early-onset cerebellar ataxia, once other well-known disorders such as Friedreich's ataxia and ataxia-telangiectasia have been excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_assertion evidence source_evidence_literature NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_assertion SIO_000772 16700949 NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_assertion wasDerivedFrom befree-20140225 NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_assertion wasGeneratedBy ECO_0000203 NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP800025.RAZJnCbv6FhxzaNd7IbO8fMuF7yIvUgv8jCvanB1IrvZ0130_provenance.