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- source_evidence_literature type ECO_0000212 NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_assertion description "[These include lamin A/C in autosomal dominant Emery-Dreifuss muscular dystrophy, SMN in spinal muscular atrophy, SIX5 in myotonic dystrophy, calpain3 in type 2A limb-girdle muscular dystrophy, PABP2 in oculopharyngeal dystrophy, androgen receptor in spinal and bulbar muscular atrophy and the ataxins in hereditary ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_assertion evidence source_evidence_literature NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_assertion SIO_000772 10838245 NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_assertion wasDerivedFrom befree-20150227 NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_assertion wasGeneratedBy ECO_0000203 NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974923.RAy1MF0Xmrm7R6TRY5psP5WSBY37T_17fQ83iqdVLBi1M130_provenance.