Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_assertion description "[Autosomal recessive hereditary inclusion body myopathy (HIBM or IBM2) is a progressive adult onset muscle wasting disorder characterized by sparing of the quadriceps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_assertion evidence source_evidence_literature NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_assertion SIO_000772 20059379 NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_assertion wasDerivedFrom befree-20140225 NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_assertion wasGeneratedBy ECO_0000203 NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP169517.RADwlwNj-ItTu6bSNZkEyTz2Bmc0bZGoFqH6Nc1hpHSb8130_provenance.