Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- befree-2016 importedOn "2016-02-19" NP521857.RACOknQBvQx5s76pOXyfdvns0VtHgja28K0altylEovdM130_provenance.
- 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.