Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_assertion description "[The candidate region was 14.7 cM flanked by D3S1620 and D3S3691, which was partly overlapping with the locus of SCA15 characterized by pure cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_assertion evidence source_evidence_literature NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_assertion SIO_000772 14981189 NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_assertion wasDerivedFrom befree-2016 NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_assertion wasGeneratedBy ECO_0000203 NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.
- befree-2016 importedOn "2016-02-19" NP432768.RA1UEpkyUsLGEqed49oBfARsI2cNt0Tp48X45AowywslE130_provenance.