Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_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." NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_assertion evidence source_evidence_curated NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_assertion SIO_000772 7920659 NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_assertion wasDerivedFrom ctd_human-20130708 NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_assertion wasGeneratedBy ECO_0000218 NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_provenance.