Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_assertion description "[Lack of sequencing validation and complexity of deletion testing hinder genetic diagnosis of SDH-associated paraganglioma/pheochromocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_assertion evidence source_evidence_literature NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_assertion SIO_000772 20153743 NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_assertion wasDerivedFrom gad-20150221 NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_assertion wasGeneratedBy ECO_0000203 NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP164455.RAzsgFHvuEs3_v7sLANTj_M0V-NtrWzdvqEEvau9cpwnk130_provenance.