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- NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_assertion type Assertion NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_head.
- NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_assertion description "[Mutations in von Hippel-Lindau tumor suppressor gene (VHL) underlie the VHL hereditary cancer syndrome and also occur in most sporadic clear cell renal cell cancers (CCRCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_provenance.
- NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_assertion evidence source_evidence_literature NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_provenance.
- NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_assertion SIO_000772 16585181 NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_provenance.
- NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_assertion wasDerivedFrom befree-20150227 NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_provenance.
- NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_assertion wasGeneratedBy ECO_0000203 NP773628.RAmCP9TumeQvHdrL7B4KTs4qrfnYQu2WVf34hKaE_xaOs130_provenance.