Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_assertion description "[Disorders caused by mutations in the ARX gene include: hydrocephaly, lissencephaly and agenesis of corpus callosum with abnormal genitalia, Partington syndrome S), X-linked infantile spasms, myoclonic epilepsy, and nonspecific mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_assertion evidence source_evidence_literature NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_assertion SIO_000772 18975239 NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_assertion wasDerivedFrom lhgdn-20090331 NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_assertion wasGeneratedBy ECO_0000203 NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP243310.RA6IQJXjD2bna2BHthQ6mKAmITgtrw8Q4qVNKCfD6KAl8130_provenance.