Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion type Assertion NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_head.
- NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion description "[Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion evidence source_evidence_literature NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion SIO_000772 24341141 NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion wasDerivedFrom befree-20150227 NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_assertion wasGeneratedBy ECO_0000203 NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.