Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_assertion description "[Mutations in genes encoding Fras1, Frem1 and Frem2 are causative for dermal-epidermal detachment in the plane of sublamina densa and have been identified in different classes of mouse bleb mutants, the murine model of human Fraser syndrome, the hallmark phenotypic characteristics of which are embryonic skin blistering, cryptophthalmos and renal agenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_assertion evidence source_evidence_literature NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_assertion SIO_000772 21182980 NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_assertion wasDerivedFrom befree-2016 NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_assertion wasGeneratedBy ECO_0000203 NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP861342.RAwh3Em7uUMWVrPVjIeSXc9g5hZNpEB5vLtGnzEQxZXDQ130_provenance.