Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP488554.RAlk9MHE6Gm21g1XPIG5-gZs5eSnAgTBOropNGT0f5omI130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488554.RAlk9MHE6Gm21g1XPIG5-gZs5eSnAgTBOropNGT0f5omI130_provenance.
• assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_provenance.
• NP299959.RAbff5pNflqRk3PAMPuIc6AUowVT1KHUhYFDnMiKfUZy4130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299959.RAbff5pNflqRk3PAMPuIc6AUowVT1KHUhYFDnMiKfUZy4130_provenance.
• NP299971.RAWXXfh3GPpfyPxleg1W_4SnnyV601mEefVLTA4PONBr4130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299971.RAWXXfh3GPpfyPxleg1W_4SnnyV601mEefVLTA4PONBr4130_provenance.
• NP300453.RAe-2b0uHuUZ1Jb4NbOMye3DRG-dTS2J0nxo4g-Htq188130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300453.RAe-2b0uHuUZ1Jb4NbOMye3DRG-dTS2J0nxo4g-Htq188130_provenance.
• NP375347.RAZD8_SuhAqzbCP2aRltKocGGVvADe-0hKoN6eRgciZ3k130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375347.RAZD8_SuhAqzbCP2aRltKocGGVvADe-0hKoN6eRgciZ3k130_provenance.
• NP375348.RAVvRpr5tFlKzcHjkGq7H2TCayT9L3HZ6U_cji29pp5ds130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375348.RAVvRpr5tFlKzcHjkGq7H2TCayT9L3HZ6U_cji29pp5ds130_provenance.
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• NP375352.RAdLkKiyrxh87qVGdIXLv4LAdj1vEXDOeZXjSO5jf_1nE130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375352.RAdLkKiyrxh87qVGdIXLv4LAdj1vEXDOeZXjSO5jf_1nE130_provenance.
• NP299981.RAscGp3MJf9BBmjSc6roghPbUId3-sbINczAFTrv8mokk130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299981.RAscGp3MJf9BBmjSc6roghPbUId3-sbINczAFTrv8mokk130_provenance.
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• NP300460.RApz1mtfN3IB3vDoe5hjv3T-oZveKCES_pDSj09iMzpS4130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300460.RApz1mtfN3IB3vDoe5hjv3T-oZveKCES_pDSj09iMzpS4130_provenance.
• NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
• NP375350.RAoHEYkGg6sb7IT7b0CfGvAxVyjSB2HlsP4p2QpK2AcIU130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375350.RAoHEYkGg6sb7IT7b0CfGvAxVyjSB2HlsP4p2QpK2AcIU130_provenance.
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