Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_assertion description "[The mutation of the p53 genes and polymorphism of the RB gene were present in 25.8% (8/31) and 12.9% (4/31) of the advanced tumours, respectively, but the mutation was not found in small HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_assertion evidence source_evidence_literature NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_assertion SIO_000772 7540433 NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_assertion wasDerivedFrom befree-2016 NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_assertion wasGeneratedBy ECO_0000203 NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311553.RAcwVIWLzhT3zlXVY5Q2QOReckom1xAR0fu-9m29ruLxY130_provenance.