Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_assertion description "[report that an autosomal recessive infantile parkinsonism-dystonia is caused by loss-of-function mutations in DAT that impair dopamine reuptake (see the related article beginning on page 1595).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_assertion evidence source_evidence_literature NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_assertion SIO_000772 19504720 NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_assertion wasDerivedFrom befree-20150227 NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_assertion wasGeneratedBy ECO_0000203 NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP698570.RAaev4kn1rV0k6Tda29xH5r0aehyecUaP8fDOTSqRKMTM130_provenance.