Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.