Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_assertion description "[Mutations of PKD1 cause autosomal dominant polycystic kidney disease (ADPKD), a syndrome characterized by kidney cysts and progressive renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_assertion evidence source_evidence_literature NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_assertion SIO_000772 19331813 NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_assertion wasDerivedFrom befree-2016 NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_assertion wasGeneratedBy ECO_0000203 NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP729369.RAj8XNl6LyH4Mvu-1WMaCP5OtM_sH58W7Nc5xLSdmfz1Q130_provenance.