Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- befree-2016 importedOn "2016-02-19" NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_assertion wasGeneratedBy ECO_0000203 NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_assertion wasDerivedFrom befree-2016 NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_assertion SIO_000772 11331249 NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_assertion evidence source_evidence_literature NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.
- NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316520.RAxqfUadSqyNj4dOROdC25ZFc0KFwy_dqwZe2pMdMVv4g130_provenance.