Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- befree-2016 importedOn "2016-02-19" NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_assertion wasGeneratedBy ECO_0000203 NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_assertion wasDerivedFrom befree-2016 NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_assertion SIO_000772 19923742 NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_assertion evidence source_evidence_literature NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.
- NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_assertion description "[Mutations in p97 have been implicated in patients with inclusion-body myopathy associated with Paget's disease of the bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776589.RAXb3p8YfSyhrdF53wfSdLJG4CDRlT6vW3hS5AVOJ8_xg130_provenance.