Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_assertion description "[Mutations in the genes for nuclear envelope proteins of emerin (EMD) and lamin A/C (LMNA) are known to cause Emery-Dreifuss muscular dystrophy (EDMD) and limb girdle muscular dystrophy (LGMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_assertion evidence source_evidence_literature NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_assertion SIO_000772 18646565 NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_assertion wasDerivedFrom befree-20150227 NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_assertion wasGeneratedBy ECO_0000203 NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP373898.RAAUiBn7RD4gAe6rDVNL6c7hqt6brhco-jhQ6Hn_JLEbk130_provenance.