Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_assertion description "[The patients with subtypes CDG-Ia and CDG-Ib have mutations in the genes encoding phosphomannomutase 2 (PMM2) and phosphomannose isomerase (MPI or PMI), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_assertion evidence source_evidence_literature NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_assertion SIO_000772 21949237 NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_assertion wasDerivedFrom befree-20140225 NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_assertion wasGeneratedBy ECO_0000203 NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813099.RAhxo0yG6QLiltGQo5WaXU6sS6FSuICGU0wT4zfTCr-ys130_provenance.