Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_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." NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_assertion evidence source_evidence_literature NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_assertion SIO_000772 19238444 NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_assertion wasDerivedFrom befree-2016 NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_assertion wasGeneratedBy ECO_0000203 NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.
- befree-2016 importedOn "2016-02-19" NP722170.RAlXCoQVSjTKXJI2Wi4eE8C553rGt0RorDB7OrnLjOgX0130_provenance.