Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_assertion wasGeneratedBy ECO_0000203 NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_assertion wasDerivedFrom befree-20150227 NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_assertion SIO_000772 24061522 NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_assertion evidence source_evidence_literature NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.
- NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_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." NP260710.RA5tvvETn9_gwa_TlWdIxyR9qUPyFVmAd3x6HB242mDX4130_provenance.