Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion type Assertion NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_head.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion evidence source_evidence_literature NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion SIO_000772 18807109 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion wasDerivedFrom befree-20150227 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion wasGeneratedBy ECO_0000203 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.