Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion description "[A retrospective study was performed to compare the detection rate of chromosomal abnormalities by different approaches of full karyotyping, rapid aneuploidy diagnosis (RAD) or both when invasive prenatal testing is performed for diagnosis of thalassaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion evidence source_evidence_literature NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion SIO_000772 16421217 NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion wasDerivedFrom befree-20140225 NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion wasGeneratedBy ECO_0000203 NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance.