Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion> ?p ?o ?g. }
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- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion type Assertion NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_head.
- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion description "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_provenance.
- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion evidence source_evidence_literature NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_provenance.
- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion SIO_000772 15955094 NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_provenance.
- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion wasDerivedFrom befree-2016 NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_provenance.
- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion wasGeneratedBy ECO_0000203 NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_provenance.