Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_assertion description "[Pheochromocytomas in multiple endocrine neoplasia type 2 (MEN-2) express phenylethanolamine N-methyltransferase (PNMT), the enzyme that catalyzes conversion of norepinephrine to epinephrine, whereas those in von Hippel-Lindau (VHL) syndrome do not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_assertion evidence source_evidence_literature NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_assertion SIO_000772 17102092 NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_assertion wasDerivedFrom befree-20140225 NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_assertion wasGeneratedBy ECO_0000203 NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP863589.RAvG9kYDw8_pCaRzgZUsXoyzX7JudjpQE3mfLKlSU3Etc130_provenance.