Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion> ?p ?o ?g. }
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- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion type Assertion NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_head.
- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion description "[The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand beyond the distinct yet overlapping phenotypes in patients with AHC, RDP, and CAPOS syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_provenance.
- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion evidence source_evidence_literature NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_provenance.
- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion SIO_000772 25447930 NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_provenance.
- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion wasDerivedFrom befree-2016 NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_provenance.
- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion wasGeneratedBy ECO_0000203 NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_provenance.