Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP1215994.RAxmlJGJTO8D6GURYWH9jDr7MSZwGxFRAhVtdQO0PoOig130_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." NP1215994.RAxmlJGJTO8D6GURYWH9jDr7MSZwGxFRAhVtdQO0PoOig130_provenance.