Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_assertion description "[Mutations in the Aristaless-related homeobox gene (ARX) are associated with a wide variety of neurologic disorders including lissencephaly, hydrocephaly, West syndrome, Partington syndrome, and X-linked intellectual disability with or without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_assertion evidence source_evidence_literature NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_assertion SIO_000772 22252899 NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_assertion wasDerivedFrom befree-20140225 NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_assertion wasGeneratedBy ECO_0000203 NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP253338.RAJWKN4dZNlBZNamc60rmrVfLe_pXpm3LN-FpogckE_7s130_provenance.