Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_assertion description "[FSHD is a common form of muscular dystrophy associated with a complex cascade of epigenetic events following reduction in copy number of D4Z4 macrosatellite repeats located on chromosome 4q35.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_assertion evidence source_evidence_literature NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_assertion SIO_000772 21829175 NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_assertion wasDerivedFrom befree-20140225 NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_assertion wasGeneratedBy ECO_0000203 NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490280.RAE0lQKujNcrj2YC3Nhb4KdeduZw_Zk9-1W6k1VUMISXA130_provenance.