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- NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_assertion type Assertion NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_head.
- NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_assertion description "[To report the clinical, genetic, neuroimaging, and neuropathologic studies of patients with the hereditary cerebral hemorrhage with amyloidosis linked to the APP E693K mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_provenance.
- NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_assertion evidence source_evidence_literature NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_provenance.
- NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_assertion SIO_000772 20697050 NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_provenance.
- NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_assertion wasDerivedFrom befree-20140225 NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_provenance.
- NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_assertion wasGeneratedBy ECO_0000203 NP457341.RAPmrIPkRxLEh3w2Y0I-miKe2EUeul109RPEerVnMdxoM130_provenance.