Matches in Nanopublications for { ?s ?p "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 9 of
9
with 100 items per page.
- NP3454.RAGBqDxKN8wOZ_zcMChg9N5Akt6JOION5wv8dLMQ94i-g130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3454.RAGBqDxKN8wOZ_zcMChg9N5Akt6JOION5wv8dLMQ94i-g130_provenance.
- NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_provenance.
- NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3930.RAQGyq2UOmDr9K2cHH26oc7eo3hnMjBk3k9eZKu1tnZuk130_provenance.
- assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522383.RANylSQ6SMJ0jKG4mTcdkH9Aeu8harMAxouuQ8JuwQT2I130_provenance.
- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_provenance.