Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_assertion description "[Like the adult form of the disorder, JHD is a hereditary neurodegenerative disease characterized by dementia and behavioral changes, caused by an expanded CAG repeat within the first exon of the huntingtin (HTT) gene on chromosome 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_assertion evidence source_evidence_literature NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_assertion SIO_000772 23390171 NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_assertion wasDerivedFrom befree-20140225 NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_assertion wasGeneratedBy ECO_0000203 NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP916863.RAJ2OU7x3Dbzv0YEyhs1FipaIN3zWpz8B5b_VbxLa_XSw130_provenance.