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- NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_assertion type Assertion NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_head.
- NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_assertion wasGeneratedBy ECO_0000203 NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_provenance.
- NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_assertion wasDerivedFrom befree-2016 NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_provenance.
- NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_assertion SIO_000772 12176944 NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_provenance.
- NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_assertion evidence source_evidence_literature NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_provenance.
- NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_assertion description "[Given the association between CVD and PXE, we hypothesized that heterozygosity of this ABCC6 mutation could also confer an increased risk for CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364626.RAVrleW1x0V65N5ru7DuOcJWbNU3_lSOwra72mDi-ago4130_provenance.