Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_assertion description "[A hexanucleotide repeat expansion in C9ORF72 causes chromosome 9p linked FTLD/ALS and is the most common cause of familial ALS accounting for about 40 % of familial cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_assertion evidence source_evidence_literature NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_assertion SIO_000772 22477152 NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_assertion wasDerivedFrom befree-2016 NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_assertion wasGeneratedBy ECO_0000203 NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.
- befree-2016 importedOn "2016-02-19" NP972750.RARTEkDeQ0FU0Qri7kf_F7GWRW83VXMDjgNV8Jl4ZFHwo130_provenance.