Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion> ?p ?o ?g. }
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- NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion type Assertion NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_head.
- NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion wasGeneratedBy ECO_0000203 NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_provenance.
- NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion wasDerivedFrom befree-20140225 NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_provenance.
- NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion SIO_000772 14691994 NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_provenance.
- NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion evidence source_evidence_literature NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_provenance.
- NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_assertion description "[The karyotype was abnormal in nine cases, including seven cases of aneuploidy (one Turner syndrome, three trisomy 18, and three trisomy 21) and two cases of structural chromosomal abnormalities (46,XX, del 4 p16.1 and 46,XX, dup1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700862.RAHxdLgoFKcjFtFf3_HwnfmGmTTbLGAs08S65SuGMdrzo130_provenance.