Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion description "[The phenotypic correlation with the mouse Herc1 and Herc2 mutants as well as the phenotypic overlap with Angelman syndrome provide further evidence that pathogenic changes in HERC2 are associated with nonsyndromic intellectual disability, autism, and gait disturbance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion evidence source_evidence_literature NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion SIO_000772 23065719 NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion wasDerivedFrom befree-20140225 NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion wasGeneratedBy ECO_0000203 NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance.