Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion> ?p ?o ?g. }
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- NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion type Assertion NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_head.
- NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion description "[The role of MKRN3, an imprinted gene located in the Prader-Willi syndrome critical region (chromosome 15q11-13), in pubertal initiation was first described in 2013 after the identification of deleterious MKRN3 mutations in five families with central precocious puberty (CPP) using whole-exome sequencing analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_provenance.
- NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion evidence source_evidence_literature NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_provenance.
- NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion SIO_000772 25957321 NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_provenance.
- NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion wasDerivedFrom befree-2016 NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_provenance.
- NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_assertion wasGeneratedBy ECO_0000203 NP1282997.RAqeaoBiK9cnilccOkpmzH0oWAR1dNmD77aDOWk3jzd1w130_provenance.