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- source_evidence_literature type ECO_0000212 NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_assertion evidence source_evidence_literature NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_assertion SIO_000772 24154603 NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_assertion wasDerivedFrom befree-20150227 NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_assertion wasGeneratedBy ECO_0000203 NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.