Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_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." NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_assertion evidence source_evidence_curated NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_assertion SIO_000772 7920659 NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_assertion wasDerivedFrom ctd_human-2016 NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_assertion wasGeneratedBy ECO_0000218 NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP36776.RANL6Koy4OSrxqQq2o1PNIlSL-U-L16Gy78bpgPrAz-9M130_provenance.