Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_assertion description "[In approximately 70% of human extraskeletal myxoid chondrosarcoma (EMC) tumors, a t(9;22) chromosome translocation gives rise to a fusion protein, named EWS/NOR1, containing the amino-terminal domain of EWS fused to the complete amino acid sequence of the nuclear receptor NOR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_assertion evidence source_evidence_literature NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_assertion SIO_000772 16112421 NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_assertion wasDerivedFrom befree-20140225 NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_assertion wasGeneratedBy ECO_0000203 NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP392687.RAQCiC6OAUhMJci9oVm7Mj-w7niKBzjgugjFTWOdl0Jgk130_provenance.