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- source_evidence_literature type ECO_0000212 NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_assertion evidence source_evidence_literature NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_assertion SIO_000772 9932941 NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_assertion wasDerivedFrom befree-20150227 NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_assertion wasGeneratedBy ECO_0000203 NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.