Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_assertion wasGeneratedBy ECO_0000218 NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_assertion wasDerivedFrom uniprot-20130724 NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_assertion SIO_000772 19283854 NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_assertion evidence source_evidence_curated NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_assertion description "[LMNA sequencing should be considered for patients presenting with dilated cardiomyopathy and hypergonadotropic hypogonadism, including those previously diagnosed with Malouf syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3836.RAUExXSgFhS1IG5l928xRzY_CA9O8ABdld9Tfg3HJUtiI130_provenance.