Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_assertion description "[Heterologous expression of these SPG43 and NBIA variants resulted in similar alterations in the subcellular distribution of C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_assertion evidence source_evidence_literature NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_assertion SIO_000772 23857908 NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_assertion wasDerivedFrom befree-2016 NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_assertion wasGeneratedBy ECO_0000203 NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1094152.RA2NNXjr9w8y504yaR5VmI0f8N650F6Z5VKrjY3jrYtOE130_provenance.