Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_assertion description "[Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_assertion evidence source_evidence_literature NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_assertion SIO_000772 18294203 NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_assertion wasDerivedFrom befree-2016 NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_assertion wasGeneratedBy ECO_0000203 NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.
- befree-2016 importedOn "2016-02-19" NP656980.RAz2F3QtjCNgNIbwBae_hk02QsFBCyRydQTMurOq2weCo130_provenance.