Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion> ?p ?o ?g. }
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- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion type Assertion NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_head.
- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_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." NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_provenance.
- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion evidence source_evidence_literature NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_provenance.
- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion SIO_000772 15955094 NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_provenance.
- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion wasDerivedFrom befree-20140225 NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_provenance.
- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion wasGeneratedBy ECO_0000203 NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_provenance.