Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_assertion description "[SDHB protein expression was absent in all 102 phaeochromocytomas and paragangliomas with an SDHB, SDHC, or SDHD mutation, but was present in all 65 paraganglionic tumours related to multiple endocrine neoplasia type 2, von Hippel-Lindau disease, and neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_assertion evidence source_evidence_literature NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_assertion SIO_000772 19576851 NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_assertion wasDerivedFrom befree-20150227 NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_assertion wasGeneratedBy ECO_0000203 NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP688771.RA3bzU5V5JLNgLrqH_tjjwCbDdqIq6AJu0_vp9gFRKHoE130_provenance.