Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion> ?p ?o ?g. }
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- NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion type Assertion NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_head.
- NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion description "[Mutations in ADCY5 should be considered in patients with undiagnosed complex movement disorders even in the absence of a family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_provenance.
- NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion evidence source_evidence_literature NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_provenance.
- NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion SIO_000772 24700542 NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_provenance.
- NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion wasDerivedFrom befree-2016 NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_provenance.
- NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_assertion wasGeneratedBy ECO_0000203 NP1170188.RAFMt5NGobYlElZdU7NNrnoLcZL6M1JW2S26JudtDH80M130_provenance.