Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_assertion description "[Mutations in the MPV17 gene have been reported in patients who came to medical attention during infancy with liver failure, hypoglycemia, failure-to-thrive and neurological symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_assertion evidence source_evidence_literature NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_assertion SIO_000772 20074988 NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_assertion wasDerivedFrom befree-20150227 NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_assertion wasGeneratedBy ECO_0000203 NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568087.RAqR-E_7GjHNhQBPGAoAPFWwMaADixZYstskxgO3ZsN-U130_provenance.