Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_assertion description "[Here, we report the central nervous system autopsy findings in a 55-year-old German patient with inclusion body myopathy and frontotemporal dementia who harbors a heterozygous R155C missense mutation residing in the N-terminal CDC48 domain of VCP, which is involved in ubiquitin binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_assertion evidence source_evidence_literature NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_assertion SIO_000772 15732117 NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_assertion wasDerivedFrom befree-20140225 NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_assertion wasGeneratedBy ECO_0000203 NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269161.RAuVqqP9Hcw8CWOC7sPKK6YAUfmSTf9LmXealhb8zjxxI130_provenance.