Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_assertion description "[Mutations of ARX are associated with a wide range of phenotypes; functional studies in the future may lend insights to the neurobiology of myoclonic seizures and infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_assertion evidence source_evidence_literature NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_assertion SIO_000772 12177367 NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_assertion wasDerivedFrom befree-20140225 NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_assertion wasGeneratedBy ECO_0000203 NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP482111.RANSqaaHWQPc6bVsJRBECExyvO0tPsozh0hvwjjY2i8E8130_provenance.