Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_assertion> ?p ?o ?g. }
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- NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_assertion type Assertion NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_head.
- NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_assertion wasGeneratedBy ECO_0000203 NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_provenance.
- NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_assertion wasDerivedFrom befree-20150227 NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_provenance.
- NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_assertion SIO_000772 21039331 NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_provenance.
- NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_assertion evidence source_evidence_literature NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_provenance.
- NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_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." NP251248.RA0sNMikCyzfuwsz9srKyplUbaHK-S2A2l8uPcuzdx1wQ130_provenance.