Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion> ?p ?o ?g. }
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- NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion type Assertion NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_head.
- NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion wasGeneratedBy ECO_0000218 NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_provenance.
- NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion wasDerivedFrom uniprot-2016 NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_provenance.
- NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion SIO_000772 12163457 NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_provenance.
- NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion evidence source_evidence_curated NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_provenance.
- NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_assertion description "[Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2183.RAkdT4u6hkQycr-AQXem7nxRhiQQKE8oIPB-2xcUdr79I130_provenance.