Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion> ?p ?o ?g. }
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- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion type Assertion NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_head.
- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion description "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion evidence source_evidence_literature NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion SIO_000772 17624596 NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion wasDerivedFrom befree-20140225 NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion wasGeneratedBy ECO_0000203 NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.