Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion> ?p ?o ?g. }
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- NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion type Assertion NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_head.
- NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion description "[Mutations in FA2H are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_provenance.
- NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion evidence source_evidence_literature NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_provenance.
- NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion SIO_000772 19068277 NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_provenance.
- NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion wasDerivedFrom lhgdn-20090331 NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_provenance.
- NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_assertion wasGeneratedBy ECO_0000203 NP152268.RAEFgrhqx2wFu8SvfZON96y2m-4h3vDQxc6bPy8HKhoeA130_provenance.