Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_assertion description "[We screened DNA from 310 patients with normosmic IHH (nIHH) and 192 healthy control subjects for sequence changes in GNRH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_assertion evidence source_evidence_literature NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_assertion SIO_000772 19567835 NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_assertion wasDerivedFrom befree-20140225 NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_assertion wasGeneratedBy ECO_0000203 NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP566618.RADGr_3ZZxvPog9bCMyk9MW-hB0tTMvlM9spPm3mwLS0E130_provenance.