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- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion type Assertion NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_head.
- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_provenance.
- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion evidence source_evidence_literature NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_provenance.
- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion SIO_000772 23615299 NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_provenance.
- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion wasDerivedFrom befree-20150227 NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_provenance.
- NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_assertion wasGeneratedBy ECO_0000203 NP470617.RA2S32Nr0Mp0iH_OUrJb2akRHmorcPg2s01bZK6AGOzgI130_provenance.