Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion type Assertion NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_head.
- NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion description "[These results confirm the association of the MTND6*LDYT14459A mutation with Leber's hereditary optic neuropathy and/or dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_provenance.
- NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion evidence source_evidence_literature NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_provenance.
- NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion SIO_000772 7654063 NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_provenance.
- NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion wasDerivedFrom befree-20150227 NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_provenance.
- NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_assertion wasGeneratedBy ECO_0000203 NP576665.RA3OL8KLeZ_NlzDwxABir82Py3Th_-mMT0ejeeRsLoGIk130_provenance.