Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion> ?p ?o ?g. }
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- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion type Assertion NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_head.
- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion description "[Based on previous reports the frequency of co-segregating recessive chloride channel (CLCN1) mutations in families with myotonic dystrophy type 2 (DM2) was suspected to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_provenance.
- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion evidence source_evidence_literature NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_provenance.
- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion SIO_000772 18807109 NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_provenance.
- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion wasDerivedFrom befree-20140225 NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_provenance.
- NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_assertion wasGeneratedBy ECO_0000203 NP169349.RACxB49AcGgMA_D0-jZ8xDq9QS1Vwt_Yg-tCPLbr--aik130_provenance.