Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_assertion evidence source_evidence_literature NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_assertion SIO_000772 16916875 NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_assertion wasDerivedFrom befree-20150227 NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_assertion wasGeneratedBy ECO_0000203 NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668606.RAV5lXb1yZR9Q2TB0bmZsOZFjhyubW4PhJj82ebQeSIcA130_provenance.