Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_assertion description "[The more common X-linked recessive form of EDMD is caused by mutations in either EMD (encoding emerin) or FHL1 (encoding four and a half LIM domains 1), while mutations in LMNA (encoding lamin A/C), SYNE1 (encoding nesprin-1) and SYNE2 (encoding nesprin-2) lead to autosomal dominant forms of the condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_assertion evidence source_evidence_literature NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_assertion SIO_000772 23456229 NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_assertion wasDerivedFrom befree-2016 NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_assertion wasGeneratedBy ECO_0000203 NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1057345.RAtAGFWmEZhG_yMugBwvSlq5kNVlnhsZTXiDdCWxGxwkQ130_provenance.