Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP188939.RAvdn_MHQ6QeUY3_ry27DOU_FzZExBi1vDpSVk1PJiQKY130_provenance.