Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_assertion evidence source_evidence_literature NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_assertion SIO_000772 8737929 NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_assertion wasDerivedFrom befree-20150227 NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_assertion wasGeneratedBy ECO_0000203 NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.