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- source_evidence_literature type ECO_0000212 NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_assertion description "[The von Hippel-Lindau (VHL) tumour suppressorgene product is believed to be involved in the down-regulation of transcriptional elongation by preventing the association of elongin B and C with the catalytic subunit elongin A. Alterations in the human VHL gene lead to VHL disease which is associated with various rare neoplasias, including haemangioblastoma of the central nervous system, retinal angioma, clear cell renal carcinoma and pheochromocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_assertion evidence source_evidence_literature NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_assertion SIO_000772 9931330 NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_assertion wasDerivedFrom befree-20150227 NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_assertion wasGeneratedBy ECO_0000203 NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP773618.RAhWNUdeWUjeMwb3Tewd_5MbPjbBLRnx4lqqX9zptr4wE130_provenance.