Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- befree-2016 importedOn "2016-02-19" NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_assertion wasGeneratedBy ECO_0000203 NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_assertion wasDerivedFrom befree-2016 NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_assertion SIO_000772 21236492 NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_assertion evidence source_evidence_literature NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.
- NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865462.RAfvy2ybfg9N2UWctH-01R3l8yHUn5cH4eQkyVmhw9mTM130_provenance.