Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_assertion description "[We demonstrated a minimal common region of loss of 10.4-Mb on 17p13 in ACCs and within this region, we found that ACADVL and ALOX15B expression are good discriminators between ACCs and ACAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_assertion evidence source_evidence_literature NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_assertion SIO_000772 18156936 NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_assertion wasDerivedFrom befree-20150227 NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_assertion wasGeneratedBy ECO_0000203 NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP236722.RAhF5KUMg2H1D0ykUAyEpXAEXLVn3I854vmy0muDSM1tY130_provenance.