Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion type Assertion NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_head.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_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." NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion evidence source_evidence_literature NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion SIO_000772 18807109 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion wasDerivedFrom gad-20150221 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion wasGeneratedBy ECO_0000203 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.