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- source_evidence_literature type ECO_0000212 NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_assertion description "[SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_assertion evidence source_evidence_literature NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_assertion SIO_000772 15965219 NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_assertion wasDerivedFrom befree-20150227 NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_assertion wasGeneratedBy ECO_0000203 NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP785698.RA_NYer9n6Cy7jTryqUoeCeGbGWTg50y_NmAuUrvpKtlA130_provenance.