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- source_evidence_literature type ECO_0000212 NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_assertion description "[Sequence analysis of SURF-1 revealed mutations in numerous DNA samples from LD(COX-) patients, indicating that this gene is responsible for the major complementation group in this important mitochondrial disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_assertion evidence source_evidence_literature NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_assertion SIO_000772 9837813 NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_assertion wasDerivedFrom befree-20150227 NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_assertion wasGeneratedBy ECO_0000203 NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP822067.RAnuykQxOlZGgG30r-3J3nx2hc85aJBGVrhcU3MY-3DLY130_provenance.