Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion> ?p ?o ?g. }
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- NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion type Assertion NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_head.
- NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion wasGeneratedBy ECO_0000203 NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_provenance.
- NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion wasDerivedFrom befree-2016 NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_provenance.
- NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion SIO_000772 21039331 NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_provenance.
- NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion evidence source_evidence_literature NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_provenance.
- NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_assertion description "[Mutations in the gene cause a rare, recessive genetic disease, pseudoxanthoma elasticum, while the loss of one ABCC6 allele is a genetic risk factor in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849491.RAZ1qbw8hMbch9yj0nS57aUJZvkV7t6TCSd10FUl_zcjI130_provenance.