Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_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." NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_assertion evidence source_evidence_literature NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_assertion SIO_000772 20153743 NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_assertion wasDerivedFrom gad-20150221 NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_assertion wasGeneratedBy ECO_0000203 NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP64962.RAMIQ4rMcKsQMn7pTTQZtdc2yFEl8zH50Q8BXih-8Kkz8130_provenance.