Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_assertion evidence source_evidence_literature NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_assertion SIO_000772 10908904 NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_assertion wasDerivedFrom befree-20140225 NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_assertion wasGeneratedBy ECO_0000203 NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- befree-20140225 importedOn "2014-02-25" NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.