Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_assertion description "[An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_assertion evidence source_evidence_literature NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_assertion SIO_000772 18651333 NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_assertion wasDerivedFrom befree-20150227 NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_assertion wasGeneratedBy ECO_0000203 NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.
- befree-20150227 importedOn "2015-02-27" NP577810.RAiNGdyL6Ongpepvu6ajkLZXKq6Hp1tRNhwJkY_jTA7is130_provenance.