Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.