Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_assertion description "[We apply the HuGE NET guidelines to search PubMed and EMBASE databases for publications investigating single nucleotide polymorphisms (SNPs) and cerebral palsy outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_assertion evidence source_evidence_literature NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_assertion SIO_000772 19238444 NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_assertion wasDerivedFrom befree-20150227 NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_assertion wasGeneratedBy ECO_0000203 NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP373339.RAeB0uzsSbMLLkGjMi046eHufxf-gQGrDWmTKIWmMdzQw130_provenance.