Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_assertion description "[We demonstrated CGH to be a powerful tool in the identification of recurrent chromosome aberrations in an AIDS-related BL and in ascertaining the origin of marker chromosomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_assertion evidence source_evidence_literature NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_assertion SIO_000772 10702812 NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_assertion wasDerivedFrom befree-20140225 NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_assertion wasGeneratedBy ECO_0000203 NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651371.RAMmeSUD_quLaBoBMmidKQ_8fY_V2O1TH_kbeUzk_8FhY130_provenance.