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- source_evidence_literature type ECO_0000212 NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_assertion wasGeneratedBy ECO_0000203 NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_assertion wasDerivedFrom befree-20140225 NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_assertion SIO_000772 17373666 NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_assertion evidence source_evidence_literature NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_assertion description "[Previous genetic studies in MBs have identified mutations in genes coding for beta-catenin and its partners, APC and AXIN1, which cause activation of Wnt signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP368886.RA_pxYNp9ik6sbnam5XE_xqyuvRl9Lout4GkqORuzBFME130_provenance.