Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_assertion evidence source_evidence_literature NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_assertion SIO_000772 16235064 NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_assertion wasDerivedFrom befree-20140225 NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_assertion wasGeneratedBy ECO_0000203 NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP296248.RA18fy877GJmakPcnVijmxVbZ7G9jVYifj8TThTtlDuJk130_provenance.