Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_assertion description "[Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_assertion evidence source_evidence_literature NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_assertion SIO_000772 11807986 NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_assertion wasDerivedFrom befree-20150227 NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_assertion wasGeneratedBy ECO_0000203 NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP850080.RATeMwajsLL0GXPnI7CGWe5AycMfDJtODBZCQjiWVf9wM130_provenance.