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- NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_assertion type Assertion NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_head.
- NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_assertion description "[Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_provenance.
- NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_assertion evidence source_evidence_curated NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_provenance.
- NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_assertion SIO_000772 7981750 NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_provenance.
- NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_assertion wasDerivedFrom uniprot-2016 NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_provenance.
- NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_assertion wasGeneratedBy ECO_0000218 NP8663.RAG_flITEcHWry539zhJQ02oqIedpiFvfTvX0wrHX6X08130_provenance.