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- NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_assertion type Assertion NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_head.
- NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_assertion wasGeneratedBy ECO_0000203 NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_provenance.
- NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_assertion wasDerivedFrom befree-2016 NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_provenance.
- NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_assertion SIO_000772 21365542 NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_provenance.
- NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_assertion evidence source_evidence_literature NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_provenance.
- NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_assertion description "[Werner's Syndrome (WS) or adult-onset progeria is an autosomal recessive disorder of accelerated aging caused by mutations of the DNA RecQ helicase/exonuclease (WRN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876500.RA5nhNK-6elSw5gCaAQPWREPnchHh33dfa2rMerYd4Msk130_provenance.