Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_assertion description "[Finally, ?-catenin gene (CTNNB1) mutations were detected in all APA cases, the single nucleotide substitutions being in the epithelial but not the stromal components.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_assertion evidence source_evidence_literature NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_assertion SIO_000772 24182564 NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_assertion wasDerivedFrom befree-20140225 NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_assertion wasGeneratedBy ECO_0000203 NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.
- befree-20140225 importedOn "2014-02-25" NP290959.RA_hB2tUcwhIQSn76gBczXlisEYhtOMJxvKsBfmIHpr40130_provenance.