Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_assertion description "[We evaluated family members from 16 pedigrees previously identified to carry LMNA mutations for the ages of onset of ECG abnormalities, CSD, or arrhythmia and of left ventricular enlargement (LVE) and/or systolic dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_assertion evidence source_evidence_literature NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_assertion SIO_000772 23582089 NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_assertion wasDerivedFrom befree-20140225 NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_assertion wasGeneratedBy ECO_0000203 NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316733.RAoWkh_pdJjahyEb_H1J4EpTk4KZWkQaVgWT2wV7_tHP4130_provenance.