Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP581868.RAB_OLGbcY9w3LF8O2t04_2w83niSwILQqy-kXORbhc_U130_provenance.