Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_assertion description "[Generation of the NUP98-HOXD13 fusion transcript by a rare translocation, t(2;11)(q31;p15), in a case of infant leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_assertion evidence source_evidence_literature NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_assertion SIO_000772 10931000 NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_assertion wasDerivedFrom befree-20140225 NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_assertion wasGeneratedBy ECO_0000203 NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.
- befree-20140225 importedOn "2014-02-25" NP630055.RA7AZCG367HmRyz7vkxtPw7dUUttvL7ThLse1KgQYlCww130_provenance.