Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion> ?p ?o ?g. }
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- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion type Assertion NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_head.
- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_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." NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_provenance.
- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion evidence source_evidence_literature NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_provenance.
- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion SIO_000772 21102408 NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_provenance.
- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion wasDerivedFrom befree-20140225 NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_provenance.
- NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_assertion wasGeneratedBy ECO_0000203 NP422328.RAc9erEHEDL0J1OyKDKWolG3ZVt8KiruSdTolVk8XSWO8130_provenance.