Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.
- 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.
- ctd_human-20150221 importedOn "2015-02-21" NP20669.RAeL3vCSaIt9ampJVui3TWI0WgZFx3cXE86Fq7GjWn4lM130_provenance.