Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_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." NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_assertion evidence source_evidence_literature NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_assertion SIO_000772 11180757 NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_assertion wasDerivedFrom befree-20150227 NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_assertion wasGeneratedBy ECO_0000203 NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.