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- source_evidence_literature type ECO_0000212 NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_assertion evidence source_evidence_literature NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_assertion SIO_000772 22532172 NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_assertion wasDerivedFrom befree-20140225 NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_assertion wasGeneratedBy ECO_0000203 NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.