Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_assertion description "[We hypothesize that alteration of DOCK1 and/or other genes involved in regulation and signaling of multiple pathways can explain the wide range of phenotypic variability between patients with similar or identical cytogenetic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_assertion evidence source_evidence_literature NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_assertion SIO_000772 19558528 NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_assertion wasDerivedFrom befree-20150227 NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_assertion wasGeneratedBy ECO_0000203 NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP358247.RA0U6p4bTC3zV5or4TkIhQPuuAwbAxj73xbz-yCUBnNOY130_provenance.