Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion> ?p ?o ?g. }
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- NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion type Assertion NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_head.
- NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion description "[X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion evidence source_evidence_curated NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion SIO_000772 7920659 NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion wasDerivedFrom ctd_human-20150221 NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_assertion wasGeneratedBy ECO_0000218 NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.