Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_assertion> ?p ?o ?g. }
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- NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_assertion type Assertion NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_head.
- NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_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." NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_provenance.
- NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_assertion evidence source_evidence_literature NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_provenance.
- NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_assertion SIO_000772 16235064 NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_provenance.
- NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_assertion wasDerivedFrom befree-20140225 NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_provenance.
- NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_assertion wasGeneratedBy ECO_0000203 NP899348.RAokGNzFKX-nk7Krcrj1e-PnbeplpkzSqge7NzDZIMmOw130_provenance.