Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_assertion wasGeneratedBy ECO_0000203 NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_assertion wasDerivedFrom befree-20140225 NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_assertion SIO_000772 21752791 NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_assertion evidence source_evidence_literature NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_assertion description "[Recently, mutations in the fused in sarcoma gene have been shown to cause familial amyotrophic lateral sclerosis and fused in sarcoma-positive neuronal inclusions have subsequently been demonstrated in neuronal intermediate filament inclusion disease and atypical frontotemporal lobar degeneration with ubiquitinated inclusions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP362848.RAX5w1-ERyTbluTq248ds_IQABxthEfDFL1D6HfBltegw130_provenance.