Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_assertion description "[Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_assertion evidence source_evidence_literature NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_assertion SIO_000772 15667412 NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_assertion wasDerivedFrom befree-2016 NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_assertion wasGeneratedBy ECO_0000203 NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP477615.RAr50AcE12U32_5AYDsKAYHHSVIYW9qFkQwW7IXNOWtKw130_provenance.