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- source_evidence_literature type ECO_0000212 NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP596513.RAhDK8SkZ0Ah-4BRkDrAjMTNs6ywLdsTcFL4UmILY34NM130_provenance.
- 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.