Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_assertion description "[Heterozygous mutations in dynamin 2 (DNM2) have been linked to dominant Charcot-Marie-Tooth neuropathy and centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_assertion evidence source_evidence_literature NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_assertion SIO_000772 23092955 NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_assertion wasDerivedFrom befree-20150227 NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_assertion wasGeneratedBy ECO_0000203 NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357019.RAacb9KU8NTdUul3U_ux9B3nXOEr6ILLyYGcqhzHpSIiw130_provenance.