Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_assertion description "[Dystonia musculorum (dt) is an autosomal recessive hereditary neuropathy with a characteristic uncoordinated movement and is caused by a defect in the bullous pemphigoid antigen 1 (BPAG1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_assertion evidence source_evidence_literature NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_assertion SIO_000772 21272373 NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_assertion wasDerivedFrom befree-2016 NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_assertion wasGeneratedBy ECO_0000203 NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.
- befree-2016 importedOn "2016-02-19" NP868220.RAa_Z7W8GXKN3qi_hodnmmR3LagtSf6x0EQF_WVszxBX0130_provenance.