Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_assertion description "[The findings indicate that C9ORF72 mutations cause some but not all cases of frontotemporal dementia with motor neuron disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_assertion evidence source_evidence_literature NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_assertion SIO_000772 22300873 NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_assertion wasDerivedFrom befree-20140225 NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_assertion wasGeneratedBy ECO_0000203 NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658001.RAIWxBvvE8CzmnBj6bUlw85FS6P7XZcScH8jLdtsCxmtg130_provenance.