Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion> ?p ?o ?g. }
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- NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_assertion type Assertion NP10219.RARZFNplcGFmEswP3IQJAVRm7KxHcVNB3ZyApDR4Cd_ng130_head.
- 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.