Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_assertion description "[Other variants (GTA 118 GTC, GCGCA-->GCACA in the 3'-noncoding region, and the number of ATT repeats in intron 2) also did not associate with CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_assertion evidence source_evidence_literature NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_assertion SIO_000772 9589253 NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_assertion wasDerivedFrom befree-20150227 NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_assertion wasGeneratedBy ECO_0000203 NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP516390.RAaNwc37-des9PkERYr4WT-OZzLKLG8b9q_i3n8R8UIJU130_provenance.