Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_assertion description "[WRN was originally identified as a gene responsible for Werner syndrome (WS; Progeria of Adults).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_assertion evidence source_evidence_literature NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_assertion SIO_000772 10984715 NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_assertion wasDerivedFrom befree-2016 NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_assertion wasGeneratedBy ECO_0000203 NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.
- befree-2016 importedOn "2016-02-19" NP294940.RAaG7vq1b0Fm2jejjp1-Ws_uKlZXBceoNvP2qC91GD6a0130_provenance.