Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion type Assertion NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_head.
- NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion wasGeneratedBy ECO_0000203 NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_provenance.
- NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion wasDerivedFrom befree-20140225 NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_provenance.
- NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion SIO_000772 17431911 NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_provenance.
- NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion evidence source_evidence_literature NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_provenance.
- NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_assertion description "[Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665889.RASCHEjYjHiL9WGxS8nC_7p-iWjYb69JQgxijhI_KCeFU130_provenance.