Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_assertion description "[Compared with patients from other families meeting the same diagnostic criteria (43 patients) and families with SPG4 (126 patients), the major form of autosomal dominant spastic paraplegia, SPG3A patients had earlier symptom onset, less frequently increased reflexes in the upper limbs, decreased vibration sense in the lower limbs, and fewer sphincter disturbances, but more frequently observed wasting in the lower limbs and scoliosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_assertion evidence source_evidence_literature NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_assertion SIO_000772 15596607 NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_assertion wasDerivedFrom befree-2016 NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_assertion wasGeneratedBy ECO_0000203 NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.
- befree-2016 importedOn "2016-02-19" NP472579.RAq8FYW4xuKlgnnmfAzo0rc6KwqpOexTAYQJyRyVSkRtA130_provenance.