Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_assertion description "[Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_assertion evidence source_evidence_literature NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_assertion SIO_000772 19068277 NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_assertion wasDerivedFrom befree-2016 NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_assertion wasGeneratedBy ECO_0000203 NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.
- befree-2016 importedOn "2016-02-19" NP708209.RAjO4y3514EXr6-4yTm1GgItIvcIS-CepQrLd2oB_URBo130_provenance.