Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion type Assertion NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_head.
- NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion description "[Mutations in CDKL5 and ARX are known causes of early-onset epilepsy and severe developmental delay in males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_provenance.
- NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion evidence source_evidence_literature NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_provenance.
- NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion SIO_000772 23583054 NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_provenance.
- NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion wasDerivedFrom befree-2016 NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_provenance.
- NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_assertion wasGeneratedBy ECO_0000203 NP1068890.RA1Rt1kqLlxHGW4x4-x--ikwy7Zn7yZ2B_PocuxfNzNsc130_provenance.