Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_assertion description "[Mutations in the human PANK2 gene have been shown to occur in autosomal-recessive pantothenate kinase-associated neurodegeneration, a syndrome originally described by Hallervorden and Spatz.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_assertion evidence source_evidence_literature NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_assertion SIO_000772 12554685 NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_assertion wasDerivedFrom befree-20140225 NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_assertion wasGeneratedBy ECO_0000203 NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP461656.RAHGCE5sNgopjJUAE2d6S8CWBw3rk29Sh3F6Hvm6Slmwc130_provenance.