Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_assertion description "[Facioscapulohumeral muscular dystrophy 1 (FSHD1) is caused by a contraction in the number of D4Z4 repeats on chromosome 4, resulting in relaxation of D4Z4 chromatin causing inappropriate expression of DUX4 in skeletal muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_assertion evidence source_evidence_literature NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_assertion SIO_000772 24755953 NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_assertion wasDerivedFrom befree-2016 NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_assertion wasGeneratedBy ECO_0000203 NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175826.RAjnu08tzvVPM6Th8GVl4AQCOSfYOm4hgWl0k5DyC6LwA130_provenance.