Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_assertion wasGeneratedBy ECO_0000203 NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_assertion wasDerivedFrom befree-20140225 NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_assertion SIO_000772 24061522 NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_assertion evidence source_evidence_literature NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_assertion description "[We conclude that CTNNB1 exon 3 mutations are likely to be involved in the pathogenesis of male SCT with nuclear accumulation of β-catenin and affect the expression of cyclin D1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP193679.RA43vA6F4WOdoO2vLZ375kXp6uHbkmapf-N_G3FelaZ3U130_provenance.