Matches in Nanopublications for { ?s ?p "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- NP864619.RAoIpCqPYgRgomXaDcCDgg4e19nOL5RoSSiFLVmWNNo2A130_assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864619.RAoIpCqPYgRgomXaDcCDgg4e19nOL5RoSSiFLVmWNNo2A130_provenance.
- assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP791227.RAiuDrWiS1EWFEug2PWdmA7N1dn69knFlzx6nSGxxV_-c130_assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791227.RAiuDrWiS1EWFEug2PWdmA7N1dn69knFlzx6nSGxxV_-c130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.