Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_assertion description "[Only two premalignant lesions showed absence of p16 expression, of which one (carcinoma in situ) was hypermethylated at the p16(INK4a) promoter region and the other (severe dysplasia) showed BMI-1 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_assertion evidence source_evidence_literature NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_assertion SIO_000772 15892997 NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_assertion wasDerivedFrom befree-20140225 NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_assertion wasGeneratedBy ECO_0000203 NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523766.RAUTKbXg2tAC5foKA5OravNNbGc4A8R0NV1HPCNvfAdXc130_provenance.