Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_assertion evidence source_evidence_literature NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_assertion SIO_000772 19578796 NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_assertion wasDerivedFrom gad-20130706 NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_assertion wasGeneratedBy ECO_0000203 NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP69893.RAe1VsAURMYf3hpe44i9l_xXt7JZQWS4rtlXdC9m_pOOo130_provenance.