Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_assertion evidence source_evidence_literature NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_assertion SIO_000772 15254020 NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_assertion wasDerivedFrom befree-20140225 NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_assertion wasGeneratedBy ECO_0000203 NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP526487.RAkofzkZ8VtEbRMYZ0TZB9MfaXXfZ_ZfeUUeyb6D-p0qQ130_provenance.