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- source_evidence_literature type ECO_0000212 NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_assertion description "[In contrast, PRRT2 mutations do not seem to be associated with CwG or BFNE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_assertion evidence source_evidence_literature NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_assertion SIO_000772 23073245 NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_assertion wasDerivedFrom befree-20150227 NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_assertion wasGeneratedBy ECO_0000203 NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963653.RAhzs66ec8j_hpoM5JUp2QmW1kIQt0wnN8Fx5An8NNhOs130_provenance.