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- source_evidence_literature type ECO_0000212 NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_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." NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_assertion evidence source_evidence_literature NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_assertion SIO_000772 17275378 NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_assertion wasDerivedFrom befree-20150227 NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_assertion wasGeneratedBy ECO_0000203 NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP762948.RA7a696NsfJCvcfQU8siJiCIVakh-wpMZXJ3cBe-poSGg130_provenance.