Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_assertion wasGeneratedBy ECO_0000203 NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_assertion wasDerivedFrom befree-20140225 NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_assertion SIO_000772 23543484 NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_assertion evidence source_evidence_literature NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_assertion description "[Our results demonstrate that the TNPO3 mutation is the cause of limb-girdle muscular dystrophy 1F, expand our knowledge of the molecular basis of muscular dystrophies and bolster the importance of defects of nuclear envelope proteins as causes of inherited myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP417448.RACnl3uV1hyD-4zH6QENRDQU_MLjd-OiPcOVvREiA6aYU130_provenance.