Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_assertion description "[Fermitin family member 1 (FERMT1, Kindlin-1) is an epithelial-specific regulator of integrin functions and is associated with Kindler syndrome, a genetic disorder characterized by skin blistering, atrophy, and photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_assertion evidence source_evidence_literature NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_assertion SIO_000772 21832234 NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_assertion wasDerivedFrom befree-2016 NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_assertion wasGeneratedBy ECO_0000203 NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.
- befree-2016 importedOn "2016-02-19" NP916197.RACsX4jIAefOPhNyImRUWDIxaCCbvakAJVT5HkOR5tKps130_provenance.