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- NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_assertion type Assertion NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_head.
- NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_assertion wasGeneratedBy ECO_0000203 NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_provenance.
- NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_assertion wasDerivedFrom befree-2016 NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_provenance.
- NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_assertion SIO_000772 20522425 NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_provenance.
- NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_assertion evidence source_evidence_literature NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_provenance.
- NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_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." NP816425.RAHvhTc1Xc3sEmr8KukSGBhyPAEDHWpInpym_3fOxNWrY130_provenance.