Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion type Assertion NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_head.
- NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion wasGeneratedBy ECO_0000203 NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_provenance.
- NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion wasDerivedFrom befree-2016 NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_provenance.
- NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion SIO_000772 10414310 NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_provenance.
- NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion evidence source_evidence_literature NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_provenance.
- NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_assertion description "[A recessive form of LQT is caused by mutations in either KVLQT1 or hminK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258173.RArfvHIvTW7hJ76bVVMY7Rco5paTSMa4el8dmolzYhFv8130_provenance.