Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_assertion description "[Subnormal UROD activity is due to mutations of the UROD gene in both f-PCT and HEP, but no mutations have been found in s-PCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_assertion evidence source_evidence_literature NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_assertion SIO_000772 8644733 NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_assertion wasDerivedFrom befree-2016 NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_assertion wasGeneratedBy ECO_0000203 NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1350831.RAPFiBgUyoLRy9F1zLYgWtOC-c_jxTh1mOHsA5lIHKRrk130_provenance.