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- source_evidence_literature type ECO_0000212 NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_assertion description "[GenoMEL, comprising major familial melanoma research groups from North America, Europe, Asia, and Australia has created the largest familial melanoma sample yet available to characterize mutations in the high-risk melanoma susceptibility genes CDKN2A/alternate reading frames (ARF), which encodes p16 and p14ARF, and CDK4 and to evaluate their relationship with pancreatic cancer (PC), neural system tumors (NST), and uveal melanoma (UM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_assertion evidence source_evidence_literature NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_assertion SIO_000772 17047042 NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_assertion wasDerivedFrom befree-20150227 NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_assertion wasGeneratedBy ECO_0000203 NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP301466.RA84JRGRR_T9j3O5EaUqI-mhT025t6uwO0BBpS4xSNWuE130_provenance.