Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_assertion wasGeneratedBy ECO_0000203 NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_assertion wasDerivedFrom befree-20140225 NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_assertion SIO_000772 10737123 NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_assertion evidence source_evidence_literature NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_assertion description "[In addition, five known missense mutations affecting the ND1 (3335 T/C, 3338 T/C), ND2 (5460 G/A), ND3 (10398 A/G), and ND5 (13966 A/G) genes as well as three secondary LHON mutations (4216 T/C, 4917 A/ G, 13708 G/A) were found in the PD group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP820617.RAR_ts8v9_jX8X0G2szETrL8ApVFHX4yW9EvHaiQI41L4130_provenance.