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- NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_assertion type Assertion NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_head.
- NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_assertion description "[In this paper, we describe a boy with a 46,Y,der(X)t(X;Y)(p22.3;q11)mat karyotype and review the genotype-phenotype correlations in three male patients with the combination of apparent lack of clinical features of CDPX1 and a partial deletion of the critical region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_provenance.
- NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_assertion evidence source_evidence_literature NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_provenance.
- NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_assertion SIO_000772 7759082 NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_provenance.
- NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_assertion wasDerivedFrom befree-20140225 NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_provenance.
- NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_assertion wasGeneratedBy ECO_0000203 NP258857.RAL7Lzi8ZINoQv5_E_qU0j9WEk9m6g4PG2H_o2RoG_FLM130_provenance.