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- NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_assertion type Assertion NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_head.
- NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_assertion wasGeneratedBy ECO_0000203 NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_provenance.
- NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_assertion wasDerivedFrom befree-20150227 NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_provenance.
- NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_assertion SIO_000772 18285834 NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_provenance.
- NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_assertion evidence source_evidence_literature NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_provenance.
- NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_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." NP816650.RAV5n7ybYYOnVqNaDcqLgI1qjudrwN_pKk7EuC6xYTD-A130_provenance.