Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_assertion description "[The detection rate of chromosomal abnormalities by four different approaches were compared: (i) karyotyping for all samples; (ii) RAD (21,18,13,X,Y) for all samples; (iii) RAD for all samples + karyotyping for cases with ultrasound abnormalities; and (iv) RAD (21,18,13) for all + RAD (X,Y) for cases with ultrasound abnormalities consistent with Turner syndrome + karyotyping for cases with ultrasound abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_assertion evidence source_evidence_literature NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_assertion SIO_000772 16421217 NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_assertion wasDerivedFrom befree-20140225 NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_assertion wasGeneratedBy ECO_0000203 NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP496673.RAr4gqtAxcYCI7ivqktb4kAhjGwIuRzhVHM3cnK2kgQBo130_provenance.