Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_assertion evidence source_evidence_literature NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_assertion SIO_000772 16806828 NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_assertion wasDerivedFrom befree-2016 NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_assertion wasGeneratedBy ECO_0000203 NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- befree-2016 importedOn "2016-02-19" NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.