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- source_evidence_literature type ECO_0000212 NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_assertion description "[While mutations in the NDUFS3 gene thus result in Leigh syndrome, a dissimilar clinical phenotype is observed in mutations in the NDUFV2 and NDUFS2 genes, resulting in encephalomyopathy and cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_assertion evidence source_evidence_literature NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_assertion SIO_000772 14729820 NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_assertion wasDerivedFrom befree-20150227 NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_assertion wasGeneratedBy ECO_0000203 NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.
- befree-20150227 importedOn "2015-02-27" NP586741.RAH27FwUuL3tNGUBU0WfA7wU-D9GrkWEeM1owgDsWO678130_provenance.