Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP777958.RAktdysPLCs-4B4XmwHpAirZ35YE3GGqxovnF68a6BBMw130_provenance.
- 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.