Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_assertion wasGeneratedBy ECO_0000218 NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_assertion wasDerivedFrom uniprot-20130724 NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_assertion SIO_000772 15328326 NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_assertion evidence source_evidence_curated NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_assertion description "[Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5850.RAm11nfSjaswkupjhkOCwKtM7W3oxUGvv4KUViX-LHs3Q130_provenance.