Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP286782.RAbKlCjeNnhd7gPbUtceaSn9dOqvNanD13TKCbtMqKMFU130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286782.RAbKlCjeNnhd7gPbUtceaSn9dOqvNanD13TKCbtMqKMFU130_provenance.
• NP473385.RAVlj1Pv0On6PTx9gdsobVgDD7no7r76mvC8fVOV7-VRs130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473385.RAVlj1Pv0On6PTx9gdsobVgDD7no7r76mvC8fVOV7-VRs130_provenance.
• assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP531241.RAZ7kYiv6tdB56IVN_3GpVCOMsym_6EkJoBEhnbJb7nnw130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531241.RAZ7kYiv6tdB56IVN_3GpVCOMsym_6EkJoBEhnbJb7nnw130_provenance.
• assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_provenance.
• NP259988.RAa9WgnvDW2nLwSuvS167tc4VNy62-Gt3sa1U4FaInJIE130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259988.RAa9WgnvDW2nLwSuvS167tc4VNy62-Gt3sa1U4FaInJIE130_provenance.
• NP330538.RAgoySdk4sQA2EHKzaF5VJQdqfGBVKOoJl9QJp7tIGVc4130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330538.RAgoySdk4sQA2EHKzaF5VJQdqfGBVKOoJl9QJp7tIGVc4130_provenance.
• NP259986.RAknema5PAJbbBR3VQoBoZGc7GseeVIpoNETcEX5nmRvw130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259986.RAknema5PAJbbBR3VQoBoZGc7GseeVIpoNETcEX5nmRvw130_provenance.
• NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
• NP530859.RA1UjsIN-D31D-USHpTIAMmVLtV4CMZ6LrwZM4YLnEYhk130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530859.RA1UjsIN-D31D-USHpTIAMmVLtV4CMZ6LrwZM4YLnEYhk130_provenance.
• NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_provenance.
• NP259987.RAyMpKF0lVEmVeR04CchcC6MQiwrIKpNSh-mYaaGZYrN4130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259987.RAyMpKF0lVEmVeR04CchcC6MQiwrIKpNSh-mYaaGZYrN4130_provenance.