Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion> ?p ?o ?g. }
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- NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion type Assertion NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_head.
- NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion wasGeneratedBy ECO_0000203 NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_provenance.
- NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion wasDerivedFrom befree-20150227 NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_provenance.
- NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion SIO_000772 18285834 NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_provenance.
- NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion evidence source_evidence_literature NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_provenance.
- NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_assertion description "[Putative loss-of-function mutations in PROKR2 or PROK2, encoding prokineticin receptor-2 (a G protein-coupled receptor), and one of its ligands, prokineticin-2, respectively, have recently been reported in approximately 10% of Kallmann syndrome affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714558.RABqBCzCxjdVkm8eIJoZ_u5wXwFwG9cM10KHmfNTBizEY130_provenance.