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- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion type Assertion NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_head.
- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_provenance.
- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion evidence source_evidence_literature NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_provenance.
- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion SIO_000772 21998596 NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_provenance.
- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion wasDerivedFrom befree-2016 NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_provenance.
- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion wasGeneratedBy ECO_0000203 NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_provenance.