Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion> ?p ?o ?g. }
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- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion type Assertion NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_head.
- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion wasGeneratedBy ECO_0000203 NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_provenance.
- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion wasDerivedFrom lhgdn-20090331 NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_provenance.
- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion SIO_000772 15492925 NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_provenance.
- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion evidence source_evidence_literature NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_provenance.
- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_provenance.