Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_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." NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_assertion evidence source_evidence_literature NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_assertion SIO_000772 19578124 NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_assertion wasDerivedFrom befree-20150227 NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_assertion wasGeneratedBy ECO_0000203 NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.