Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_assertion description "[SCA2 shows the highest worldwide prevalence in Cuban population, which is therefore a unique source for studying the relationship between the frequency of large and intermediate alleles and the frequency of SCA2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_assertion evidence source_evidence_literature NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_assertion SIO_000772 21934711 NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_assertion wasDerivedFrom befree-2016 NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_assertion wasGeneratedBy ECO_0000203 NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.
- befree-2016 importedOn "2016-02-19" NP925258.RAbFagJooj81F_QnNfNl4vKoQfL33ZB3MuF21frCGu81M130_provenance.