Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- befree-2016 importedOn "2016-02-19" NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_assertion wasGeneratedBy ECO_0000203 NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_assertion wasDerivedFrom befree-2016 NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_assertion SIO_000772 17525480 NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_assertion evidence source_evidence_literature NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_assertion description "[An intriguing hypothesis proposes that mutations of RET, NF1, VHL, or SDH predispose to hereditary pheochromocytoma/ paraganglioma by causing defective apoptotic culling of cells that would normally be destroyed during embryogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.