Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_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." NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_assertion evidence source_evidence_literature NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_assertion SIO_000772 15952209 NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_assertion wasDerivedFrom befree-2016 NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_assertion wasGeneratedBy ECO_0000203 NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.
- befree-2016 importedOn "2016-02-19" NP499195.RAoISP_2CWsDXcAQZx7jSVksUfZYTl0zxL6yTIJqFpZwk130_provenance.