Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_assertion description "[Recently, forms of syndromic and nonspecific X-linked mental retardation have been found to be associated with mutations in the Aristaless-related homeobox gene ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_assertion evidence source_evidence_literature NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_assertion SIO_000772 12874405 NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_assertion wasDerivedFrom befree-2016 NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_assertion wasGeneratedBy ECO_0000203 NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.
- befree-2016 importedOn "2016-02-19" NP402768.RAbW024xGOyhbDfl26sc4N_ZvrkDbWeFd9NBsSzCz1tRI130_provenance.