Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_assertion description "[Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_assertion evidence source_evidence_curated NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_assertion SIO_000772 11438993 NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_assertion wasDerivedFrom uniprot-20130724 NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_assertion wasGeneratedBy ECO_0000218 NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.