Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_assertion description "[Although all previously reported mutations in the SURF1 gene have been found in patients with cytochrome oxidase (COX)-deficient Leigh syndrome, the phenotype associated with SURF1 protein deficiency should be extended to include leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_assertion evidence source_evidence_literature NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_assertion SIO_000772 11409433 NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_assertion wasDerivedFrom befree-20150227 NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_assertion wasGeneratedBy ECO_0000203 NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720625.RAKrxmuP4IX0c_sPNhf89HTu0RdpVh2-NxA4WrlTGJLg0130_provenance.