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- NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_assertion type Assertion NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_head.
- NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_assertion wasGeneratedBy ECO_0000203 NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_provenance.
- NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_assertion wasDerivedFrom befree-20140225 NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_provenance.
- NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_assertion SIO_000772 20522425 NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_provenance.
- NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_assertion evidence source_evidence_literature NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_provenance.
- NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_assertion description "[Methods In this context, a search was undertaken for mutations in LMNA, encoding Lamins A/C, and ZMPSTE24, LBR, LMNB1, LMNB2, MAN1, SYNE1a and LAP2, encoding Lamins A/C molecular partners, in a Caucasian woman affected with Reynolds syndrome, a particular nosologic entity specifically associating limited cutaneous SSc and primary biliary cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741367.RALH-5p0CNtEzSpL5CXe8En1RHy56SyL0-XSqlfRxM-kk130_provenance.