Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP212259.RAWG5Utgvd-WtfhAdzCiGjnBLLHJbxACSOGAJv87MAW2Q130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212259.RAWG5Utgvd-WtfhAdzCiGjnBLLHJbxACSOGAJv87MAW2Q130_provenance.
• NP552545.RABQ3krLz0hxjERRPNHUIlinIQ0AB-qNYYkiZGX3sivAA130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552545.RABQ3krLz0hxjERRPNHUIlinIQ0AB-qNYYkiZGX3sivAA130_provenance.
• NP694468.RAmxEAjI-jEh5cdfYG8Oj500uYJX_pzNUbrcrQTYpHfrs130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694468.RAmxEAjI-jEh5cdfYG8Oj500uYJX_pzNUbrcrQTYpHfrs130_provenance.
• NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
• NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_provenance.
• NP616162.RAwXCwMXCotBxZ1b-4B3Lc9I7nDdyOACK4KUCO0wDBK3E130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616162.RAwXCwMXCotBxZ1b-4B3Lc9I7nDdyOACK4KUCO0wDBK3E130_provenance.
• NP716452.RA3dz7o9wW4hfFbGdipwxjxUYEwpczAsjGbNAHTH39fZQ130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716452.RA3dz7o9wW4hfFbGdipwxjxUYEwpczAsjGbNAHTH39fZQ130_provenance.
• NP963792.RATtp31Pcqff4Euo9Jq-ovS9UfZFrV8yg-EwOTmzN1398130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963792.RATtp31Pcqff4Euo9Jq-ovS9UfZFrV8yg-EwOTmzN1398130_provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP963629.RAMMV-h6zitiqJ5aSYYYIS-rj3IQt8LbV0rBH1UPSrOQ0130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963629.RAMMV-h6zitiqJ5aSYYYIS-rj3IQt8LbV0rBH1UPSrOQ0130_provenance.
• NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
• NP1051801.RAGGdIBfkQSOGzZWCLiZSnWjtwBK8gWtkqHfK8EdZX8tU130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051801.RAGGdIBfkQSOGzZWCLiZSnWjtwBK8gWtkqHfK8EdZX8tU130_provenance.
• NP1051803.RAMxBjl9Y4parwdHGGA3cfv2tq1ML5sgtSCj_1Nb_DVk4130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051803.RAMxBjl9Y4parwdHGGA3cfv2tq1ML5sgtSCj_1Nb_DVk4130_provenance.
• NP1051804.RAJynt5riTcj1FjXAPn4oxZpPqbCxrutwYkq304TjVVgA130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051804.RAJynt5riTcj1FjXAPn4oxZpPqbCxrutwYkq304TjVVgA130_provenance.
• NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_provenance.