Matches in Nanopublications for { ?s ?p "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP616728.RAWKs9n8nyNtDAcJwn5mT8D6jvS-eaW5Kz3eyHHoaeueY130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616728.RAWKs9n8nyNtDAcJwn5mT8D6jvS-eaW5Kz3eyHHoaeueY130_provenance.
- NP796661.RA11CKSWIQXWITM1XISdYhrXzAl71Cg5XmeDqsSKSq8ho130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796661.RA11CKSWIQXWITM1XISdYhrXzAl71Cg5XmeDqsSKSq8ho130_provenance.
- NP358318.RAXLcTeZMsyaiBFX8d3bEZd4cg__VV7yvagWEhvE-n66k130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358318.RAXLcTeZMsyaiBFX8d3bEZd4cg__VV7yvagWEhvE-n66k130_provenance.
- NP860109.RAwSzq8YyDpwC6Zq3FeM4HTxbQcmqP0oC6VQ-jwC2Mx40130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860109.RAwSzq8YyDpwC6Zq3FeM4HTxbQcmqP0oC6VQ-jwC2Mx40130_provenance.
- NP852264.RAezih3YM-tJV7WA1F0YL73AwiE6s1Jed37dJRUngYGss130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852264.RAezih3YM-tJV7WA1F0YL73AwiE6s1Jed37dJRUngYGss130_provenance.
- NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_provenance.
- NP986495.RAAtmodE7i5Tm9mSLzlV4ggy93F3jHJ7L97ptEivl8n4w130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986495.RAAtmodE7i5Tm9mSLzlV4ggy93F3jHJ7L97ptEivl8n4w130_provenance.
- NP986496.RAAfrVviEEDbulCoi2viuI8kqsrBT1ldn61pfASGt1uBk130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986496.RAAfrVviEEDbulCoi2viuI8kqsrBT1ldn61pfASGt1uBk130_provenance.
- NP1002338.RAEoKa6CRp0W6P3W0cTt70ODR1BDjxQ9Lqa0ppoZnQAI0130_assertion description "[Smith-Magenis syndrome (SMS), manifesting obesity and hypercholesterolemia, results from a deletion CNV at 17p11.2, but is sometimes due to haploinsufficiency of a single gene, RAI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002338.RAEoKa6CRp0W6P3W0cTt70ODR1BDjxQ9Lqa0ppoZnQAI0130_provenance.