Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_provenance.
• NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_provenance.
• NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
• NP838330.RAXcp_pvPASPfrG-gfhKm1XU36ALA1knWMzwGBZawWS1E130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838330.RAXcp_pvPASPfrG-gfhKm1XU36ALA1knWMzwGBZawWS1E130_provenance.
• assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP978867.RAgPBPHuO09XykjqaxgkhikGJgexL5KOlrJdyjY6VJZjA130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978867.RAgPBPHuO09XykjqaxgkhikGJgexL5KOlrJdyjY6VJZjA130_provenance.
• NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.