Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_assertion wasGeneratedBy ECO_0000203 NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_assertion wasDerivedFrom befree-20140225 NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_assertion SIO_000772 17525480 NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_assertion evidence source_evidence_literature NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_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." NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.