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- NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_assertion type Assertion NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_head.
- NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_assertion wasGeneratedBy ECO_0000203 NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_provenance.
- NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_assertion wasDerivedFrom befree-20150227 NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_provenance.
- NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_assertion SIO_000772 9748047 NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_provenance.
- NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_assertion evidence source_evidence_literature NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_provenance.
- NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705589.RA-VEBbWMlZFU33NJ2PV_mGbGWGJOYhy0_t2UBvbu8HPY130_provenance.