Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion type Assertion NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_head.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_provenance.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion evidence source_evidence_literature NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_provenance.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion SIO_000772 21102408 NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_provenance.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion wasDerivedFrom befree-20140225 NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_provenance.
- NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_assertion wasGeneratedBy ECO_0000203 NP668487.RA5-y-CcAQ92XJBQ1avSpp5gw4CHJSkS93VHCje_Je0l0130_provenance.