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- source_evidence_literature type ECO_0000212 NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP692262.RAON1F0o-SjsDvbTEV77bk7uliCrIi-fBz7iAVYgHfcqc130_provenance.