Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_assertion description "[All the novel mutations (R523T, S515L and D530G) were detected in a region of CYP1B1 that did not harbor any of the 34 point mutations implicated in PCG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_assertion evidence source_evidence_literature NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_assertion SIO_000772 16688110 NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_assertion wasDerivedFrom befree-2016 NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_assertion wasGeneratedBy ECO_0000203 NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP549193.RAVkaq-iLIjQQu2mgctd87CXed2Vu86hpjWl3NjeeiTJ8130_provenance.