Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_assertion evidence source_evidence_literature NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_assertion SIO_000772 18195150 NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_assertion wasDerivedFrom befree-20150227 NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_assertion wasGeneratedBy ECO_0000203 NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP833540.RANV4O3U8mNptCeI0yHDdM1rYL8jLyCymMwQ9sI5ft3yA130_provenance.