Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_assertion wasGeneratedBy ECO_0000203 NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_assertion wasDerivedFrom befree-20150227 NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_assertion SIO_000772 23561550 NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_assertion evidence source_evidence_literature NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.
- NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_assertion description "[Recent studies suggest that this shortening of the D4Z4 array leads to aberrant expression of double homeobox protein 4 (DUX4) and causes FSHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013406.RAIg2TpjjWdblGcPiQy-HpR4pkwLWdqp71GQAg7NsgMk0130_provenance.