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- source_evidence_literature type ECO_0000212 NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_assertion description "[In order to identify recurrent chromosomal regions of gain and loss, as well as novel gene targets of potential importance for MFH development and/or progression, we have analysed DNA copy number changes in 33 MFHs using microarray-based comparative genomic hybridisation (array CGH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_assertion evidence source_evidence_literature NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_assertion SIO_000772 21085701 NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_assertion wasDerivedFrom befree-20150227 NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_assertion wasGeneratedBy ECO_0000203 NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470534.RASnzN2Qw1dj-4CLkLch-_ATKKeryonjtj9ep0HsDqERk130_provenance.