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- source_evidence_literature type ECO_0000212 NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_assertion evidence source_evidence_literature NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_assertion SIO_000772 19578124 NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_assertion wasDerivedFrom befree-2016 NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_assertion wasGeneratedBy ECO_0000203 NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
- befree-2016 importedOn "2016-02-19" NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.