Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_assertion wasGeneratedBy ECO_0000203 NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_assertion wasDerivedFrom befree-2016 NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_assertion SIO_000772 7682102 NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_assertion evidence source_evidence_literature NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.
- NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_assertion description "[The regions of allelic deletion on chromosome 11 (11pter-p13), 17 (17pter-p11.2), and 13 (13q) encompass known tumour suppressor loci (WTI, TP53, RBI) which must therefore be candidates for genes contributing to MTC and Pheo development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1317943.RAqy4LDMnc8EPNTlvZw6AAI9Vu8K1uKh6q86fVhQ5crbU130_provenance.