Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_provenance.
• NP868494.RAaM1ZrTOuyDJZTKSJ6hn1ntEgHh8c5JVe4Wa5MzaQ4eI130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868494.RAaM1ZrTOuyDJZTKSJ6hn1ntEgHh8c5JVe4Wa5MzaQ4eI130_provenance.
• NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
• assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_provenance.
• NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
• NP864159.RAIFtZtp1W2z7Wyfuly5P2j30lvgdgFmvlA9GYtsLJot8130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864159.RAIFtZtp1W2z7Wyfuly5P2j30lvgdgFmvlA9GYtsLJot8130_provenance.
• NP294754.RAebzxcq4wvCkR9cPlzajpj6zYd_8FqaeIzVFBAQg3nes130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294754.RAebzxcq4wvCkR9cPlzajpj6zYd_8FqaeIzVFBAQg3nes130_provenance.
• NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
• NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_provenance.
• NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_provenance.
• NP294752.RAJ_a6Ykel46dMSORBfXzHk6zFD0dLzGuOZrkT96MS8ZE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294752.RAJ_a6Ykel46dMSORBfXzHk6zFD0dLzGuOZrkT96MS8ZE130_provenance.
• NP294753.RAJwy2nC4ZErs4uMfkIOcmcPpOb3ptvoxaLnqqOvjnDiE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294753.RAJwy2nC4ZErs4uMfkIOcmcPpOb3ptvoxaLnqqOvjnDiE130_provenance.