Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_assertion description "[Guided by the identification of the SLC3A1 amino acid-transport gene on chromosome 2, we recently established genetic linkage of cystinuria to chromosome 2p in 17 families, without evidence for locus heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_assertion evidence source_evidence_literature NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_assertion SIO_000772 7539209 NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_assertion wasDerivedFrom befree-20140225 NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_assertion wasGeneratedBy ECO_0000203 NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP249712.RAJWYuc4ebMF0LtfgsWe7XVoG0_UWS3v9X2KhvQ_3kzmo130_provenance.