Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion> ?p ?o ?g. }
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- NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion type Assertion NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_head.
- NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion description "[Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_provenance.
- NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion evidence source_evidence_curated NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_provenance.
- NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion SIO_000772 19508969 NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_provenance.
- NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion wasDerivedFrom ctd_human-20130708 NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_provenance.
- NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_assertion wasGeneratedBy ECO_0000218 NP32065.RAwDXaVx2J8HantO0Nl18e9yMTAXU__ORye5T2XrygTkA130_provenance.