Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_assertion description "[Thus, a defect in the phosphatidylinositol pathway leading to a decrease in synthesis of PIP(2), a molecule active in endocytosis of synaptic vesicle proteins, culminates in lethal congenital arthrogryposis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_assertion evidence source_evidence_literature NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_assertion SIO_000772 17701898 NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_assertion wasDerivedFrom befree-20140225 NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_assertion wasGeneratedBy ECO_0000203 NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP877702.RA37ObNUfHN93C9KnVaV2fJ6B3W7WaQ5bfkxigAVqOSXk130_provenance.