Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_assertion description "[We aimed to determine the regional pattern of brain atrophy associated with the C9ORF72 gene mutation, and to determine which regions best differentiate C9ORF72 from subjects with mutations in tau and progranulin, and from sporadic frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_assertion evidence source_evidence_literature NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_assertion SIO_000772 22366795 NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_assertion wasDerivedFrom befree-2016 NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_assertion wasGeneratedBy ECO_0000203 NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.
- befree-2016 importedOn "2016-02-19" NP963477.RAp76HRmHhRVTcHrWpGy1ycXcVX9t4y9DVAsQkOLocquc130_provenance.