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- source_evidence_literature type ECO_0000212 NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_assertion description "[In addition, one of 15 PNETs retained heterozygosity but demonstrated a somatic CGT to TGT transition (arg to cys) at codon 273. p53 mutations were absent in other histologic subtypes and in two cases with multiple primary cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_assertion evidence source_evidence_literature NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_assertion SIO_000772 7565304 NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_assertion wasDerivedFrom befree-20150227 NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_assertion wasGeneratedBy ECO_0000203 NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP766545.RAvgU_asDfrFU02Ph8yqiryo_si0jMiOedmi006g_hjK0130_provenance.