Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_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." NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_assertion evidence source_evidence_literature NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_assertion SIO_000772 16682683 NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_assertion wasDerivedFrom befree-2016 NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_assertion wasGeneratedBy ECO_0000203 NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.
- befree-2016 importedOn "2016-02-19" NP548720.RAcg9V2Ux_h_SXXenWb02aooewxy7aFUdktTUvEj6EiL0130_provenance.