Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP337142.RAA5uB8qGAVHBjgf4empbQ8RA9OgJ9qL1pU_fQfqy3yIk130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337142.RAA5uB8qGAVHBjgf4empbQ8RA9OgJ9qL1pU_fQfqy3yIk130_provenance.
• NP365414.RAxfyTq5b1_MxEz5Jx7O7vI33v1idN8bdPuanfQg_va24130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365414.RAxfyTq5b1_MxEz5Jx7O7vI33v1idN8bdPuanfQg_va24130_provenance.
• NP352868.RASxY7qICQmjgRlYBqWgSTlKOsUA3hh12g5qxkuwgNr3w130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352868.RASxY7qICQmjgRlYBqWgSTlKOsUA3hh12g5qxkuwgNr3w130_provenance.
• NP917822.RAWNmZWGKef1mbR_iZWWwOUxQmeIpWITgxUYG0mydWO0Q130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917822.RAWNmZWGKef1mbR_iZWWwOUxQmeIpWITgxUYG0mydWO0Q130_provenance.
• NP356490.RAGuY_jGy60PhFRMN26YjkjEyNJJZQ7dd3WO7ZKt8Ciz0130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356490.RAGuY_jGy60PhFRMN26YjkjEyNJJZQ7dd3WO7ZKt8Ciz0130_provenance.
• NP409697.RAHYUk5lCuPj2v_Ji4QojFXxaFLAKoMcNUlL09BgNYnls130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409697.RAHYUk5lCuPj2v_Ji4QojFXxaFLAKoMcNUlL09BgNYnls130_provenance.
• assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP299788.RA45yqtmZ9wTbJ7CacHP8_S6aSSNiMIRPSuLUEzkAB9B4130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299788.RA45yqtmZ9wTbJ7CacHP8_S6aSSNiMIRPSuLUEzkAB9B4130_provenance.
• NP753556.RAwRmnG8zxkP_IbDyhoKoSzRrIXXFE-WyP3WRonO7k5E0130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753556.RAwRmnG8zxkP_IbDyhoKoSzRrIXXFE-WyP3WRonO7k5E0130_provenance.
• NP366848.RA3YrQPD-I1d7BUv-3PaeUD2I4xDQ1KeXOVjTbB2hSYQo130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366848.RA3YrQPD-I1d7BUv-3PaeUD2I4xDQ1KeXOVjTbB2hSYQo130_provenance.
• NP1045462.RAGe8AyH6_ZwBFDTPCZzVVMubzPIjVwwSL2rEsAZafB4A130_assertion description "[Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, craniosynostosis and additional minor malformations, but males are usually more mildly affected with hypertelorism as the only feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045462.RAGe8AyH6_ZwBFDTPCZzVVMubzPIjVwwSL2rEsAZafB4A130_provenance.