Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_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." NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_assertion evidence source_evidence_literature NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_assertion SIO_000772 21949237 NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_assertion wasDerivedFrom befree-20150227 NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_assertion wasGeneratedBy ECO_0000203 NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP567192.RAKwZ9UfTinLiy9C-eONChd1iltVzYtml3Lls2c_RsfFg130_provenance.