Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_assertion description "[This study reports a novel 24-bp in-frame deletion within exon 2 of the ARX gene in a male child with X-linked mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_assertion evidence source_evidence_literature NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_assertion SIO_000772 17641262 NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_assertion wasDerivedFrom lhgdn-20090331 NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_assertion wasGeneratedBy ECO_0000203 NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP227391.RAIKru__sfZRHHJwV8d_i1AkbIIyIcuuAJTDD2-2qxWm0130_provenance.