Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_assertion description "[Defects in NADH:ubiquinone oxidoreductase, the complex I of the mitochondrial respiratory chain represents the most frequent cause of mitochondrial diseases and is associated with a wide clinical spectrum varying from severe lactic acidosis in infants to muscle weakness in adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_assertion evidence source_evidence_literature NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_assertion SIO_000772 17275378 NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_assertion wasDerivedFrom befree-20140225 NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_assertion wasGeneratedBy ECO_0000203 NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP763181.RAKgerV_XfF0GLiLjbFXE4lmJzWooYm3-iSE61at3CXxU130_provenance.