Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion> ?p ?o ?g. }
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- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion type Assertion NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_head.
- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_provenance.
- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion evidence source_evidence_literature NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_provenance.
- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion SIO_000772 19157930 NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_provenance.
- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion wasDerivedFrom befree-20150227 NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_provenance.
- NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_assertion wasGeneratedBy ECO_0000203 NP798769.RAhXVVQqgzZojMZ5kl6jah_ntA40F3Qcpja5f57J_b_b0130_provenance.