Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_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." NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_assertion evidence source_evidence_literature NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_assertion SIO_000772 19567835 NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_assertion wasDerivedFrom befree-20140225 NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_assertion wasGeneratedBy ECO_0000203 NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615071.RAIyOrcPQ4dGvhfhyaM23NEmh0Zp5LHtLF6txQj8quAOs130_provenance.