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- source_evidence_literature type ECO_0000212 NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion description "[A polymorphism in exon 13 of the P2X7 receptor gene at the +1513 position (Glu496Ala substitution, corresponding to SNP rs3751143) has been shown to eradicate the function of this receptor and has been correlated with histological variants and clinical parameters in thyroid cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion evidence source_evidence_literature NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion SIO_000772 25178922 NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion wasDerivedFrom befree-2016 NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion wasGeneratedBy ECO_0000203 NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance.