Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_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." NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_assertion evidence source_evidence_literature NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_assertion SIO_000772 17624596 NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_assertion wasDerivedFrom befree-2016 NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_assertion wasGeneratedBy ECO_0000203 NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.