Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion> ?p ?o ?g. }
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- NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion type Assertion NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_head.
- NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion wasGeneratedBy ECO_0000203 NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion wasDerivedFrom befree-2016 NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion SIO_000772 16278265 NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion evidence source_evidence_literature NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_assertion description "[A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.