Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_assertion description "[Phenotypic variability was observed among patients with the same mutations, particularly the presence and age of onset of hypocortisolism, the levels of PRL and the results of pituitary imaging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_assertion evidence source_evidence_literature NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_assertion SIO_000772 16984240 NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_assertion wasDerivedFrom befree-20150227 NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_assertion wasGeneratedBy ECO_0000203 NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP610661.RAGfiJVSbERQkk5e6Wvep0r92WbZ67OjrElnGisG0J5vE130_provenance.