Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion type Assertion NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_head.
- NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion description "[PROMM (proximal myotonic myopathy) and DM2 (myotonic dystrophy Type 2) are autosomal dominant multisystem disorders that have both been linked to chromosome 3q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion evidence source_evidence_literature NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion SIO_000772 15261229 NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion wasDerivedFrom befree-20140225 NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_assertion wasGeneratedBy ECO_0000203 NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.