Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_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." NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion evidence source_evidence_literature NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion SIO_000772 17959774 NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion wasDerivedFrom lhgdn-20090331 NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion wasGeneratedBy ECO_0000203 NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.