Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion> ?p ?o ?g. }
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- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion type Assertion NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_head.
- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion description "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion evidence source_evidence_literature NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion SIO_000772 11180757 NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion wasDerivedFrom befree-2016 NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion wasGeneratedBy ECO_0000203 NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.