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- NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_assertion type Assertion NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_head.
- NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_assertion wasGeneratedBy ECO_0000203 NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_assertion wasDerivedFrom befree-20150227 NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_assertion SIO_000772 21365542 NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_assertion evidence source_evidence_literature NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_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." NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.