Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion wasGeneratedBy ECO_0000203 NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion wasDerivedFrom befree-20140225 NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion SIO_000772 18628314 NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion evidence source_evidence_literature NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion description "[Since facioscapulohumeral muscular dystrophy (FSHD) is an inherited myopathy characterised by altered splicing of mRNAs encoding muscle specific proteins, we have studied the splicing pattern of FXR1 mRNA in myoblasts and myotubes of FSHD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance.