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- NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_assertion type Assertion NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_head.
- NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_assertion wasGeneratedBy ECO_0000203 NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_provenance.
- NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_assertion wasDerivedFrom befree-20150227 NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_provenance.
- NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_assertion SIO_000772 21658225 NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_provenance.
- NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_assertion evidence source_evidence_literature NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_provenance.
- NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_assertion description "[The identification of a large spectrum of MLL2 mutations possibly offers the opportunity to improve the actual knowledge on the clinical basis of this multiple congenital anomalies/mental retardation syndrome, design functional studies to understand the molecular mechanisms underlying this disease, establish genotype-phenotype correlations and improve clinical management.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829926.RA7AIe3cJWbdIRCvVxeJe_36Ah8F2e7M101n6oAXHVTTI130_provenance.