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- NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_assertion type Assertion NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_head.
- 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.
- NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_assertion evidence source_evidence_literature NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_provenance.
- NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_assertion SIO_000772 22654670 NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_provenance.
- NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_assertion wasDerivedFrom befree-2016 NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_provenance.
- NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_assertion wasGeneratedBy ECO_0000203 NP986489.RASrV5axpjqcacp-eNY3bSyDNjHO3297vYjcgzVCCTmq4130_provenance.