Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_assertion description "[Autosomal recessive spastic paraplegia with thinning of corpus callosum (ARHSP-TCC) is a complex form of HSP initially described in Japan but subsequently reported to have a worldwide distribution with a particular high frequency in multiple families from the Mediterranean basin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_assertion evidence source_evidence_literature NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_assertion SIO_000772 19105190 NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_assertion wasDerivedFrom befree-2016 NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_assertion wasGeneratedBy ECO_0000203 NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.
- befree-2016 importedOn "2016-02-19" NP710863.RAiAT_UR1YbTfWqO2GIQe8UkUAYfMyY5S9r2-0xD6B4c8130_provenance.