Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_assertion description "[Mutations in the Aristaless-related homeobox gene, ARX, have been a cause of X-linked mental retardation (XLMR) and are responsible for a vast phenotypic spectrum including syndromic and non-syndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_assertion evidence source_evidence_literature NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_assertion SIO_000772 17613295 NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_assertion wasDerivedFrom befree-2016 NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_assertion wasGeneratedBy ECO_0000203 NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP618735.RAJVDUqqGGnxYKVrwRpN_Dd8YXXh5NWPZW3OOH2xOlbGc130_provenance.