Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion wasGeneratedBy ECO_0000218 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion wasDerivedFrom uniprot-2016 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion SIO_000772 8136837 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion evidence source_evidence_curated NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion description "[Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.