Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_assertion description "[Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_assertion evidence source_evidence_curated NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_assertion SIO_000772 15643618 NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_assertion wasDerivedFrom uniprot-20150221 NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_assertion wasGeneratedBy ECO_0000218 NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2270.RAUcx_-1_WTbrxPGgg1ZJn4wGYKrtAZT6lz-aLDK47txs130_provenance.