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- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion type Assertion NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_head.
- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion wasGeneratedBy ECO_0000203 NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_provenance.
- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion wasDerivedFrom befree-20140225 NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_provenance.
- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion SIO_000772 1773535 NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_provenance.
- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion evidence source_evidence_literature NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_provenance.
- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion description "[All of them have a balanced reciprocal translocation (46,XY or XX, t(7;9) (q11.21;p12) or (46,XY or XX, t(7;9) (p11.2;q12)), but no other members of the family have either the EEC syndrome or chromosome abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_provenance.