Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion> ?p ?o ?g. }
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- NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion type Assertion NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_head.
- NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion description "[This region contains the genes of FAM84A, NBAS, DDX1, MYCNOS and MYCN, of which haploinsufficiency or mutations of the MYCN gene is associated with Feingold syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion evidence source_evidence_literature NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion SIO_000772 22842076 NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion wasDerivedFrom befree-20140225 NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_assertion wasGeneratedBy ECO_0000203 NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.