Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_assertion description "[Genetic variants of OCTN2, for example, reduce uptake of carnitine, leading to heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_assertion evidence source_evidence_literature NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_assertion SIO_000772 21641380 NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_assertion wasDerivedFrom befree-2016 NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_assertion wasGeneratedBy ECO_0000203 NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.
- befree-2016 importedOn "2016-02-19" NP899399.RA59tlWQ-_bCHI2Pe_Or0NWB_6WBLc06V252y8yR5AlCo130_provenance.