Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_assertion description "[These findings confirm that genetic variability in HTR(2A) contributes a small but significant degree of risk for the expression of TD, particularly in older patients and specifically for the non-orofacial (limb-truncal) type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_assertion evidence source_evidence_literature NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_assertion SIO_000772 15857569 NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_assertion wasDerivedFrom befree-2016 NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_assertion wasGeneratedBy ECO_0000203 NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.
- befree-2016 importedOn "2016-02-19" NP491860.RAgMwKlN8344WqfwuQD_7nfSnyXOr7MdrNAEuD1w4TKrk130_provenance.