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- source_evidence_literature type ECO_0000212 NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_assertion description "[Analysis of frozen and fixed material from 21 CCS and 21 MM showed the presence of the V600E BRAF mutation in 2/12 EWSR1+ and 3/9 EWSR1- CCS and 9/21 MM and demonstrated a significant (P < 0.001) correlation between the gain of chromosomes 22 and 8 and EWSR1- CCS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_assertion evidence source_evidence_literature NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_assertion SIO_000772 22045652 NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_assertion wasDerivedFrom befree-2016 NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_assertion wasGeneratedBy ECO_0000203 NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.
- befree-2016 importedOn "2016-02-19" NP935465.RAHve_dQzv_gf3vwlVLShblXhhfirw8jCVsE0zpwVOHko130_provenance.