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- source_evidence_literature type ECO_0000212 NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_assertion description "[Our data associated the R349L and R190W mutations in LMNA with severe forms of familial DC. LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease. Isolated left ventricular noncompactio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_assertion evidence source_evidence_literature NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_assertion SIO_000772 15219508 NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_assertion wasDerivedFrom gad-20150221 NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_assertion wasGeneratedBy ECO_0000203 NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.