Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_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." NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_assertion evidence source_evidence_literature NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_assertion SIO_000772 18646565 NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_assertion wasDerivedFrom lhgdn-20090331 NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_assertion wasGeneratedBy ECO_0000203 NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP213516.RAW7oyM2NfFdud-peCanLMMessC6k89kvzqT8XQyL7P4o130_provenance.