Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_assertion description "[Three siblings in their sixth and seventh decade with hexosaminidase A and B deficiency (adult form of GM2-gangliosidosis, variant O) developed early and severe sensory loss in addition to chronic motor neuron disease and cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_assertion evidence source_evidence_literature NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_assertion SIO_000772 8530938 NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_assertion wasDerivedFrom befree-20150227 NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_assertion wasGeneratedBy ECO_0000203 NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446029.RAvNBBHgqyBnP6t32kXbJGsXG_wIebtTU8PhzHOhcxZLc130_provenance.