Matches in Nanopublications for { ?s ?p "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_provenance.
- NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- NP628870.RA00JEpwDPtfomKuqfsLqzTczeMfPW5EtqrBXo56Gj60s130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628870.RA00JEpwDPtfomKuqfsLqzTczeMfPW5EtqrBXo56Gj60s130_provenance.
- assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP715728.RAUssxOm_3tKmAb2wRekegNPzCoqS3I90UEpOcOyVrFAE130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715728.RAUssxOm_3tKmAb2wRekegNPzCoqS3I90UEpOcOyVrFAE130_provenance.
- NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_provenance.
- NP715726.RAmKG4ZctMa85cq00lnAY8SeR61y1_sdLPmkNhTvUOGIc130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715726.RAmKG4ZctMa85cq00lnAY8SeR61y1_sdLPmkNhTvUOGIc130_provenance.