Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_assertion description "[We identified NOTCH1 or NOTCH2 mutations in ~75% of cutaneous SCCs and in a lesser fraction of lung SCCs, defining a spectrum for the most prevalent tumor suppressor specific to these epithelial malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_assertion evidence source_evidence_literature NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_assertion SIO_000772 22006338 NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_assertion wasDerivedFrom befree-20140225 NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_assertion wasGeneratedBy ECO_0000203 NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718809.RAvu3v0vGetG6x8_EI4b_vMVjT7m79MgJDUXmTS8dJ2VE130_provenance.