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- NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_assertion type Assertion NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_head.
- NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_assertion wasGeneratedBy ECO_0000203 NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_provenance.
- NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_assertion wasDerivedFrom befree-20140225 NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_provenance.
- NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_assertion SIO_000772 21039331 NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_provenance.
- NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_assertion evidence source_evidence_literature NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_provenance.
- NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_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." NP347876.RA3i0IHCKnKkSHrIOpz3i_HZj24Nm-raj8XbTmRrot1BY130_provenance.