Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_assertion description "[The identification of a second mutation in SNAP29 in the present study definitely establishes a causal relationship between defective function of SNAP29 and the pleiotropic manifestations of CEDNIK syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_assertion evidence source_evidence_literature NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_assertion SIO_000772 21073448 NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_assertion wasDerivedFrom befree-20140225 NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_assertion wasGeneratedBy ECO_0000203 NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP664196.RAnpZQPQrBonkNoX2IPob-MM9o_KPZB29pA03g58e5AmY130_provenance.