Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion description "[Autosomal recessive Robinow syndrome is caused by mutations in ROR2 and is characterized by short stature, mesomelic limb shortening, brachydactyly, vertebral abnormalities, and a characteristic `fetal face` dysmorphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion evidence source_evidence_literature NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion SIO_000772 15952209 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion wasDerivedFrom befree-20140225 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion wasGeneratedBy ECO_0000203 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.