Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_assertion description "[Loss-of-function mutations of the KAL1 gene are a known cause of Kallmann syndrome, a disorder characterized by the coexistence of hypogonadotropic hypogonadism and anosmia/hiposmia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_assertion evidence source_evidence_literature NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_assertion SIO_000772 25339597 NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_assertion wasDerivedFrom befree-2016 NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_assertion wasGeneratedBy ECO_0000203 NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.