Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion type Assertion NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_head.
- NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion wasGeneratedBy ECO_0000203 NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_provenance.
- NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion wasDerivedFrom befree-2016 NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_provenance.
- NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion SIO_000772 24039054 NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_provenance.
- NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion evidence source_evidence_literature NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_provenance.
- NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_assertion description "[Severe congenital lipodystrophy and a progeroid appearance: Mutation in the penultimate exon of FBN1 causing a recognizable phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1110911.RAZQgUy1wDEEqQq7SPaUP2klBoL66uwx9Io63BvHgd59k130_provenance.