Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_assertion type Assertion NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_head.
- NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_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." NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_provenance.
- NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_assertion evidence source_evidence_literature NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_provenance.
- NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_assertion SIO_000772 16235064 NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_provenance.
- NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_assertion wasDerivedFrom befree-2016 NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_provenance.
- NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_assertion wasGeneratedBy ECO_0000203 NP518631.RAD0eX0zEpL3ncxDfuZdhMDIPVy6gyUTJuLQfIjf5GPpY130_provenance.