Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_assertion description "[Mutations in human AHI1 underlie the autosomal recessive Joubert Syndrome with brain malformation and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_assertion evidence source_evidence_literature NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_assertion SIO_000772 16773125 NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_assertion wasDerivedFrom befree-2016 NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_assertion wasGeneratedBy ECO_0000203 NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.
- befree-2016 importedOn "2016-02-19" NP554488.RAAT5R6xN6Dcr5xsql7NlcmzaW7nqiyK8ClirQVBF5jt0130_provenance.