Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_assertion description "[Alterations of the 3p14 fragile site containing the fragile histidine triade gene and of the 9p21 tumor suppressor locus containing methylthioadenosine phosphorylase, p16 and p15 characteristically occur in oral leukoplakia, a known precursor of OSCC, and are at present considered to indicate the transition from simple keratosis (hyperplasia) to dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_assertion evidence source_evidence_literature NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_assertion SIO_000772 18163473 NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_assertion wasDerivedFrom befree-2016 NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_assertion wasGeneratedBy ECO_0000203 NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.
- befree-2016 importedOn "2016-02-19" NP647453.RA1RmtgtsSh7I80MaiRtU8QoXvSBt-6NlSlOGhnLQX75c130_provenance.