Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_assertion description "[Therefore, the pseudoautosomal region 1 (PAR1) of 80 patients with LWD, in whom SHOX deletions and mutations had been excluded, was screened for deletions by use of a new panel of microsatellite markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_assertion evidence source_evidence_literature NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_assertion SIO_000772 16175500 NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_assertion wasDerivedFrom befree-20140225 NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_assertion wasGeneratedBy ECO_0000203 NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP283544.RATusVFIYbGVhsXHcqlMGU0R9HLzoNrNxRHdOZR54MUAc130_provenance.