Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_assertion> ?p ?o ?g. }
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- NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_assertion type Assertion NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_head.
- NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_assertion wasGeneratedBy ECO_0000203 NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_provenance.
- NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_assertion wasDerivedFrom befree-2016 NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_provenance.
- NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_assertion SIO_000772 18285834 NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_provenance.
- NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_assertion evidence source_evidence_literature NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_provenance.
- NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_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." NP656335.RANlieCzIch88u9y_EbAQRqoApKfuQcF6vWnBRJZtJ5wQ130_provenance.