Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_assertion description "[From the eighteen reported population-based case control studies of HTR1B to multiple disorders, several facts stand out.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_assertion evidence source_evidence_literature NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_assertion SIO_000772 12437478 NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_assertion wasDerivedFrom befree-20140225 NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_assertion wasGeneratedBy ECO_0000203 NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP856322.RAMV_AMrLdHOyD878p4OHl5a6J4jvu_eh9UdgQ5q6SJJU130_provenance.