Matches in Nanopublications for { ?s ?p "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1294752.RART-mAwGf8uxoN5RI0quJ_q9AHTt2ILzgWnjhn9nAgBE130_assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294752.RART-mAwGf8uxoN5RI0quJ_q9AHTt2ILzgWnjhn9nAgBE130_provenance.
- NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1294751.RAEwt4Fb_wV2UTznctrtceDwQohMTmSTSAs8lQPh0vbIM130_assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294751.RAEwt4Fb_wV2UTznctrtceDwQohMTmSTSAs8lQPh0vbIM130_provenance.
- NP1294754.RAwaRw2LociRPzyC_9Gr0DWXvW3zAHhBuObtex7UKkpUg130_assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294754.RAwaRw2LociRPzyC_9Gr0DWXvW3zAHhBuObtex7UKkpUg130_provenance.