Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion type Assertion NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_head.
- NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion description "[X-linked hydrocephalus, MASA syndrome and certain forms of X-linked spastic paraplegia and agenesis of corpus callosum are now known to be due to mutations in the gene for the neural cell adhesion molecule L1 (19, 30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_provenance.
- NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion evidence source_evidence_literature NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_provenance.
- NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion SIO_000772 9266556 NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_provenance.
- NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion wasDerivedFrom befree-20140225 NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_provenance.
- NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_assertion wasGeneratedBy ECO_0000203 NP298983.RAhMXC07ktzmJjZUZE6pUb8BjcRtONKadUralACDY1_U0130_provenance.