Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_assertion type Assertion NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_head.
- NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_assertion wasGeneratedBy ECO_0000203 NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_provenance.
- NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_assertion wasDerivedFrom befree-20140225 NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_provenance.
- NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_assertion SIO_000772 20522425 NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_provenance.
- NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_assertion evidence source_evidence_literature NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_provenance.
- NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_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." NP627513.RA_4gHOQRZofcrC6e8000Bvt6iMsR2nz7ra_bPCIkCF1k130_provenance.