Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_assertion description "[We have reported dominant and recessive inheritance of parkinsonism, mitochondrial myopathy, and premature amenorrhea in five ethnically distinct families with POLG1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_assertion evidence source_evidence_literature NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_assertion SIO_000772 17846414 NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_assertion wasDerivedFrom befree-20150227 NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_assertion wasGeneratedBy ECO_0000203 NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP633418.RA_62ks01rAZ8kjOT2yV_lfFcweAazR_lmLt8gDgjRpBI130_provenance.