Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_assertion description "[Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_assertion evidence source_evidence_curated NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_assertion SIO_000772 10980531 NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_assertion wasDerivedFrom uniprot-2016 NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_assertion wasGeneratedBy ECO_0000218 NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1011.RAJJcb5wLi6TFVDhQ9uVjmNcJ7PmkCtV9aTws9VJ7B9Zs130_provenance.