Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_assertion description "[Mutations in the lamin A/C gene determine a heterogeneous group of congenital diseases, termed laminopathies, consisting of more than 15 phenotypes, including autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_assertion evidence source_evidence_literature NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_assertion SIO_000772 20837309 NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_assertion wasDerivedFrom befree-20140225 NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_assertion wasGeneratedBy ECO_0000203 NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP643033.RAFwDCyWhZgx0NJNvmuOyu1aE-d0dmskRdNDeXcOGkUWs130_provenance.