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- source_evidence_literature type ECO_0000212 NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_assertion description "[Importantly, where studied, mainly prostate and breast cancers, the dominant VGSC (Nav1.7 and Nav1.5, respectively) was found to be an embryonic/neonatal splice variant, consistent with the gene expression being 'oncofoetal.' In breast cancer, the molecular difference between the adult and neonatal isoforms of the VGSC/Nav1.5 is largest (31 base pairs, generating 7 amino acid differences).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_assertion evidence source_evidence_literature NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_assertion SIO_000772 19835862 NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_assertion wasDerivedFrom befree-20150227 NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_assertion wasGeneratedBy ECO_0000203 NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683498.RAqR1nx_0RH-lXTbZJnM_mINT_FUWv6g4RbJ_OwvCjOAM130_provenance.