Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_assertion description "[A mutation in the B-box region of TRIM32 has also been shown to result in a more pleiotropic disorder, Bardet-Biedl Syndrome (BBS11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_assertion evidence source_evidence_literature NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_assertion SIO_000772 21496629 NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_assertion wasDerivedFrom befree-20140225 NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_assertion wasGeneratedBy ECO_0000203 NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP780757.RA3XJhWbG11781TLeIGP9T3wLXAHVM0y0I58cFmDZhQQQ130_provenance.