Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_assertion evidence source_evidence_literature NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_assertion SIO_000772 12011143 NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_assertion wasDerivedFrom befree-2016 NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_assertion wasGeneratedBy ECO_0000203 NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- befree-2016 importedOn "2016-02-19" NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.