Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP191506.RAgDSZtfQetmmi_1pJxghzE0mrxK7bQLGw8p5pRsb6eWE130_provenance.