Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_assertion evidence source_evidence_literature NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_assertion SIO_000772 11749051 NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_assertion wasDerivedFrom lhgdn-20090331 NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_assertion wasGeneratedBy ECO_0000203 NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.