Matches in Nanopublications for { ?s ?p "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1223.RACO6u_37kN_JPVnhu9HlzcqwGWIhJ5crhVzQK5VPz0Eg130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1223.RACO6u_37kN_JPVnhu9HlzcqwGWIhJ5crhVzQK5VPz0Eg130_provenance.
- NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- NP1220.RAFLtIEVDFriGmxt3cf-Fk4P-oU1UIZ061fHQnF0f1jZI130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1220.RAFLtIEVDFriGmxt3cf-Fk4P-oU1UIZ061fHQnF0f1jZI130_provenance.
- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_provenance.
- assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP446815.RA-1s9Qu_LStfYXrR5ayn0-xm4a8XeC_qp3t5mk9OZJJI130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446815.RA-1s9Qu_LStfYXrR5ayn0-xm4a8XeC_qp3t5mk9OZJJI130_provenance.
- NP6809.RAMV6imFYiZbcy1PMggPvrP4KO-sDm3rva8mCr6vEFrsk130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6809.RAMV6imFYiZbcy1PMggPvrP4KO-sDm3rva8mCr6vEFrsk130_provenance.