Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_assertion description "[POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_assertion evidence source_evidence_literature NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_assertion SIO_000772 16682683 NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_assertion wasDerivedFrom befree-20140225 NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_assertion wasGeneratedBy ECO_0000203 NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP408139.RA_5GAH8Mad5gxt02tQNobO5FQQTEL_n8Col445RmRZNc130_provenance.