Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion> ?p ?o ?g. }
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- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion type Assertion NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_head.
- 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.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion evidence source_evidence_literature NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion SIO_000772 20125191 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion wasDerivedFrom befree-20150227 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion wasGeneratedBy ECO_0000203 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.