Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_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." NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_assertion evidence source_evidence_literature NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_assertion SIO_000772 19238444 NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_assertion wasDerivedFrom befree-20140225 NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_assertion wasGeneratedBy ECO_0000203 NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381151.RArKi0j8qSxXKn5W3RjB3FTspo2n_Omxw5mpjc527S1fo130_provenance.