Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_assertion description "[Sp4 hypomorphic mice could therefore serve as a genetic model to investigate impaired NMDA functions resulting from loss-of-function mutations of human SP4 gene in schizophrenia and/or other psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_assertion evidence source_evidence_literature NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_assertion SIO_000772 20634195 NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_assertion wasDerivedFrom befree-2016 NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_assertion wasGeneratedBy ECO_0000203 NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.
- befree-2016 importedOn "2016-02-19" NP826383.RAhV1FfGCGMD-_iUvcsXzGLDg2V2iWLtdjzJzQHPWdsNw130_provenance.