Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_assertion evidence source_evidence_literature NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_assertion SIO_000772 18796596 NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_assertion wasDerivedFrom befree-20140225 NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_assertion wasGeneratedBy ECO_0000203 NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.