Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_assertion description "[In particular, seven cases of a t(8;13)(p11;q12.1) rearrangement have been noted in patients with an atypical myeloproliferative disorder associated with T-cell leukemia and eosinophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_assertion evidence source_evidence_literature NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_assertion SIO_000772 9066924 NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_assertion wasDerivedFrom befree-20140225 NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_assertion wasGeneratedBy ECO_0000203 NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297768.RAzDdN-Inzm5lmvnWAmRVG5WDH2lLvapn8rlVNBvI_gmc130_provenance.