Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_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." NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_assertion evidence source_evidence_literature NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_assertion SIO_000772 22221392 NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_assertion wasDerivedFrom befree-20140225 NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_assertion wasGeneratedBy ECO_0000203 NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP659674.RA-WaHLH3LFE-ld_nBQNZB6RtHDAN1bT1ER2bwchPI8QI130_provenance.