Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion> ?p ?o ?g. }
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- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion type Assertion NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_head.
- 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.