Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_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." NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_assertion evidence source_evidence_literature NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_assertion SIO_000772 19068277 NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_assertion wasDerivedFrom lhgdn-20090331 NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_assertion wasGeneratedBy ECO_0000203 NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP244350.RApxMgC-8kJrOEFyDhDpP7ezfp42bQyVkf0IwL9BDYMO8130_provenance.