Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_assertion description "[31 different germline FH mutations in 56 families with Hereditary leiomyomatosis and renal cell cancer (HLRCC) (20 missense, eight frameshifts, two nonsense, and one splice site) was indentified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_assertion evidence source_evidence_literature NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_assertion SIO_000772 15937070 NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_assertion wasDerivedFrom lhgdn-20090331 NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_assertion wasGeneratedBy ECO_0000203 NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP214814.RAJ5TnYxTYQ7-NkGffMDbQtkRv-wjhBNLmB9PFIHvFbyY130_provenance.