Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_assertion evidence source_evidence_literature NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_assertion SIO_000772 16317258 NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_assertion wasDerivedFrom befree-20140225 NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_assertion wasGeneratedBy ECO_0000203 NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.