Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_assertion description "[The structure of human alpha-GAL brings Fabry disease into the realm of molecular diseases, where insights into the structural basis of the disease phenotypes might help guide the clinical treatment of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_assertion evidence source_evidence_literature NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_assertion SIO_000772 15003450 NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_assertion wasDerivedFrom befree-2016 NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_assertion wasGeneratedBy ECO_0000203 NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.
- befree-2016 importedOn "2016-02-19" NP434388.RAgEgQnEmkjawx6Fs1AcSCsF9vd4y8VIbfSfLzKE0laLY130_provenance.