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- source_evidence_literature type ECO_0000212 NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_assertion description "[Lysinuric protein intolerance (LPI) is an autosomal recessive disorder caused by mutations in cationic amino acid transporter gene SLC7A7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_assertion evidence source_evidence_literature NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_assertion SIO_000772 22221392 NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_assertion wasDerivedFrom befree-20140225 NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_assertion wasGeneratedBy ECO_0000203 NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.
- befree-20140225 importedOn "2014-02-25" NP186571.RA8FDtwaqthYmk5uL-m4g9wEWHnLCzeuFip9h3h-MH764130_provenance.