Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion type Assertion NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_head.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_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." NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_provenance.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion evidence source_evidence_literature NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_provenance.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion SIO_000772 17624596 NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_provenance.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion wasDerivedFrom befree-2016 NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_provenance.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion wasGeneratedBy ECO_0000203 NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_provenance.