Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_assertion description "[The proportion of NPC cases attributable to the GG CCND1 genotype was 14.76%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_assertion evidence source_evidence_literature NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_assertion SIO_000772 16691558 NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_assertion wasDerivedFrom gad-20150221 NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_assertion wasGeneratedBy ECO_0000203 NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100546.RAUDpa5uYzCdTM3MlmNslEPMVDl8zFqOz3P6bjxD4mwqc130_provenance.