Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_assertion description "[Our study describes a novel role of FXR1P that has crucial implications for the understanding of its role during myogenesis and muscle development, since we show here that in its absence a reduced number of myoblasts will be available for muscle formation/regeneration, shedding new light into the pathophysiology of FSHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_assertion evidence source_evidence_literature NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_assertion SIO_000772 23555284 NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_assertion wasDerivedFrom befree-2016 NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_assertion wasGeneratedBy ECO_0000203 NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1066300.RA2WjV1IAAo33-W65b0wUlpTKv_U0YfpqfuT1hUSa0ZOU130_provenance.