Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_assertion description "[The detection of additional disease-causing PKD1 mutations will help in identifying the location of the important functional regions of polycystin-1 and help us to better understand the pathophysiology of ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_assertion evidence source_evidence_curated NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_assertion SIO_000772 10729710 NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_assertion wasDerivedFrom uniprot-2016 NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_assertion wasGeneratedBy ECO_0000218 NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP698.RACRh5ENX-bD96hTf0mvJmEgGL8YhhOokhmfAT0KbhZH4130_provenance.