Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion> ?p ?o ?g. }
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- NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion type Assertion NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_head.
- NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion description "[We have previously established that all the missense mutations causing Robinow syndrome in ROR2 are retained in the endoplasmic reticulum and therefore concluded that their loss of function is due to a defect in their intracellular trafficking.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion evidence source_evidence_literature NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion SIO_000772 17665217 NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion wasDerivedFrom befree-20140225 NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_assertion wasGeneratedBy ECO_0000203 NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.