Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_assertion description "[Our data suggests that the CCND1 GG(870) genotype is associated with increased susceptibility to OSCC. The involvement of cyclin D1 polymorphism in mechanisms of SCC development may differ in the different sub-sites of the head and neck.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_assertion evidence source_evidence_literature NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_assertion SIO_000772 15695117 NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_assertion wasDerivedFrom gad-20150221 NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_assertion wasGeneratedBy ECO_0000203 NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.
- gad-20150221 importedOn "2015-02-21" NP57257.RA1pgbXDNdlcDal9aLR42sReNVjuwFO6l1LLjBHrC9i6o130_provenance.