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- source_evidence_literature type ECO_0000212 NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_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." NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_assertion evidence source_evidence_literature NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_assertion SIO_000772 15596607 NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_assertion wasDerivedFrom befree-20150227 NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_assertion wasGeneratedBy ECO_0000203 NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710046.RAcEXJ4M7GthW1H3X3QYaWc4a4nn_P3--3VjBpncs_cBk130_provenance.