Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_assertion description "[Cerebellar signs or cerebellar atrophy on brain imaging were the most frequent additional features in patients with SPG7 HSP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_assertion evidence source_evidence_literature NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_assertion SIO_000772 16534102 NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_assertion wasDerivedFrom befree-2016 NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_assertion wasGeneratedBy ECO_0000203 NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP539956.RAYZHFOojBf4dTVZ1a11BVMPdt_yWkbphgV753OWKrcJ4130_provenance.