Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_assertion description "[The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_assertion evidence source_evidence_literature NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_assertion SIO_000772 17412732 NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_assertion wasDerivedFrom befree-2016 NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_assertion wasGeneratedBy ECO_0000203 NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.
- befree-2016 importedOn "2016-02-19" NP603095.RAej4GDQVH_tZ8LDAsoWluGQBhPc1G892M4gRa6z14Rdc130_provenance.