Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_assertion description "[The pPNETs show t(11;22)(q24;q12) or t(21;22)(q22;q12) chromosomal translocations fusing the EWS gene from 22q12 with either the FL11 gene on 11q24 or the ERG gene on 21q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_assertion evidence source_evidence_literature NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_assertion SIO_000772 8577710 NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_assertion wasDerivedFrom befree-2016 NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_assertion wasGeneratedBy ECO_0000203 NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1346408.RAQM-TczME_4GieVHSlNHz1t_skf9DHJRxK5lnFOHbC4w130_provenance.