Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion evidence source_evidence_literature NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion SIO_000772 17959774 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion wasDerivedFrom lhgdn-20090331 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion wasGeneratedBy ECO_0000203 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.