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- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion type Assertion NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_head.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion description "[Autosomal recessive Robinow syndrome (OMIM 268310) is a condition caused by mutations in the ROR2 gene, the receptor tyrosine kinase-like orphan receptor 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion evidence source_evidence_literature NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion SIO_000772 22178368 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion wasDerivedFrom befree-20150227 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion wasGeneratedBy ECO_0000203 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.