Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_assertion description "[We localized a gene causing Hartnup disorder to chromosome 5p15.33 and cloned a new gene, SLC6A19, in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_assertion evidence source_evidence_literature NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_assertion SIO_000772 15286788 NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_assertion wasDerivedFrom befree-20140225 NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_assertion wasGeneratedBy ECO_0000203 NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP416875.RA_Bu0I4a_Rcq4Aadepb1hgeuoqDLF29XLjhBOpj2FQBE130_provenance.