Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_assertion description "[Identification of one novel mutation in the C-propeptide of COL2A1 in a Chinese family with spondyloperipheral dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_assertion evidence source_evidence_literature NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_assertion SIO_000772 23545312 NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_assertion wasDerivedFrom befree-20140225 NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_assertion wasGeneratedBy ECO_0000203 NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717669.RApvv-iyTSnSBPWr5cqJ02HMeaswcV4G94RetR77szikU130_provenance.