Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_assertion> ?p ?o ?g. }
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- NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_assertion type Assertion NP21309.RA-B7a_YorO2ZEOHroUmeN_96d9PfS0GQwDlxqFj4pz40130_head.
- 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.