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- NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_assertion type Assertion NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_head.
- NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_assertion wasGeneratedBy ECO_0000203 NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_assertion wasDerivedFrom befree-20150227 NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_assertion SIO_000772 11575598 NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_assertion evidence source_evidence_literature NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_assertion description "[We studied 3 members of a family who each had leukoencephalopathy on neuroimaging studies and a characteristic mutation for CADASIL in the notch 3 region of chromosome 19q12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.