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- source_evidence_literature type ECO_0000212 NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_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." NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_assertion evidence source_evidence_literature NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_assertion SIO_000772 22477152 NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_assertion wasDerivedFrom befree-2016 NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_assertion wasGeneratedBy ECO_0000203 NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.
- befree-2016 importedOn "2016-02-19" NP972751.RAZ98htnRZDSb_nR_sLBwqXwH0RPUouq34pF2hX9BgUME130_provenance.