Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion> ?p ?o ?g. }
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- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion type Assertion NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_head.
- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_provenance.
- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion evidence source_evidence_literature NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_provenance.
- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion SIO_000772 12676894 NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_provenance.
- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion wasDerivedFrom befree-20140225 NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_provenance.
- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion wasGeneratedBy ECO_0000203 NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_provenance.