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- source_evidence_literature type ECO_0000212 NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- befree-2016 importedOn "2016-02-19" NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_assertion wasGeneratedBy ECO_0000203 NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_assertion wasDerivedFrom befree-2016 NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_assertion SIO_000772 17622780 NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_assertion evidence source_evidence_literature NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.
- NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_assertion description "[Recently, mutations in the valosin-containing protein gene (VCP) were found to be causative for a rare form of dementia [Watts GDJ, et al.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619445.RA_VtW_T2_IkzcyfJXRXLSJy3X5VIHSwWl__eqvAX83N8130_provenance.