Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion description "[Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion evidence source_evidence_curated NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion SIO_000772 10909851 NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion wasDerivedFrom ctd_human-20150221 NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion wasGeneratedBy ECO_0000218 NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_provenance.