Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_assertion description "[These results extend our previous observations and indicate that defects in XPCC cause Xeroderma pigmentosum group C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_assertion evidence source_evidence_curated NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_assertion SIO_000772 8298653 NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_assertion wasDerivedFrom uniprot-20150221 NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_assertion wasGeneratedBy ECO_0000218 NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3207.RAzEBYetqvC3AGIEhyfWIp03J5LOUG3etF5WJmY20FReg130_provenance.