Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion type Assertion NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_head.
- NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion description "[Sorsby's fundus dystrophy (SFD) is an autosomal dominant retinal degeneration caused by mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_provenance.
- NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion evidence source_evidence_curated NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_provenance.
- NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion SIO_000772 7550309 NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_provenance.
- NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion wasDerivedFrom uniprot-20130724 NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_provenance.
- NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_assertion wasGeneratedBy ECO_0000218 NP6600.RASPjDa78-93G3nfk0E-3AKn3dV94T6sLphs5lnE9ltXI130_provenance.