Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP20616.RAf_Wq6yo865XTpYKgZvnkVbrQX1SmCGtXevxlgmfVh1U130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20616.RAf_Wq6yo865XTpYKgZvnkVbrQX1SmCGtXevxlgmfVh1U130_provenance.
• assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP20615.RADrLwyMBgVAA9o_sncMAFQ_GB0f2yUmHb1YqWRmZnvZU130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20615.RADrLwyMBgVAA9o_sncMAFQ_GB0f2yUmHb1YqWRmZnvZU130_provenance.
• NP20617.RAAwQMWGA5DR5v3Wwl4kXuwrUE3ENShPoWEJ6Fqz-WtG0130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20617.RAAwQMWGA5DR5v3Wwl4kXuwrUE3ENShPoWEJ6Fqz-WtG0130_provenance.
• NP446889.RAzLmrUfHA3YT4VU2SRVaWIk5GuHD5He372S1ZupHsLSY130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446889.RAzLmrUfHA3YT4VU2SRVaWIk5GuHD5He372S1ZupHsLSY130_provenance.
• NP722686.RA1yYPUNX2djugYonvqeF56bK8P-SIE5j4_DyLeXlH638130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722686.RA1yYPUNX2djugYonvqeF56bK8P-SIE5j4_DyLeXlH638130_provenance.
• NP686291.RA8BcfVXbv4Niza3LZqTGHX2DTj2oJ-Ki5fqRFex7Lx-E130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686291.RA8BcfVXbv4Niza3LZqTGHX2DTj2oJ-Ki5fqRFex7Lx-E130_provenance.
• NP19924.RA4x6e9tVk8myc0vSXJ0zIX9onMXnJbOHve3J86NrFnkM130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19924.RA4x6e9tVk8myc0vSXJ0zIX9onMXnJbOHve3J86NrFnkM130_provenance.
• NP228688.RA51MXdR41T9cxCQoSWU_c3zLPVUkeZzUPsDQEZufeH9M130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228688.RA51MXdR41T9cxCQoSWU_c3zLPVUkeZzUPsDQEZufeH9M130_provenance.
• NP228599.RAGgTWSAMxjbi_gpCnnTdzMEegt1XFJjljb-NZ_OZivH4130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228599.RAGgTWSAMxjbi_gpCnnTdzMEegt1XFJjljb-NZ_OZivH4130_provenance.
• NP355551.RAZpyTyXwADj-LXbGzxAkWuWIhrC0Pvr31k_nvRaM9WS0130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355551.RAZpyTyXwADj-LXbGzxAkWuWIhrC0Pvr31k_nvRaM9WS0130_provenance.
• NP355550.RAEVzCpXxPrJPr3Sp6nz947cXmbIledGDuihP6BtT327A130_assertion description "[Our findings revealed a unique phenotype with highly penetrant deafness, posterior embryotoxon, and congenital heart defects but with variable expressivity in a large kindred, which demonstrates that mutation in JAG1 can cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355550.RAEVzCpXxPrJPr3Sp6nz947cXmbIledGDuihP6BtT327A130_provenance.