Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_assertion description "[Finally, discovery of a shared activation of the hypoxic response in pheochromocytomas with mutations in VHL and SDH genes and uncovering of a common JunB-mediated apoptosis defect in the major hereditary groups of pheochromocytoma have provided a mechanistic basis for the clinical similarities between these distinct syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_assertion evidence source_evidence_literature NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_assertion SIO_000772 16357557 NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_assertion wasDerivedFrom befree-2016 NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_assertion wasGeneratedBy ECO_0000203 NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.
- befree-2016 importedOn "2016-02-19" NP527160.RARBU37L8-1ZgPfQbZd4FzFF0g_0L3BT0m5fiV2yeh_I0130_provenance.