Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_assertion evidence source_evidence_literature NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_assertion SIO_000772 19006241 NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_assertion wasDerivedFrom befree-20150227 NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_assertion wasGeneratedBy ECO_0000203 NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.