Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_assertion description "[Mutation in the alpha-synuclein gene and sporadic Parkinson's disease, Alzheimer's disease, and dementia with lewy bodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_assertion evidence source_evidence_literature NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_assertion SIO_000772 9743579 NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_assertion wasDerivedFrom befree-2016 NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_assertion wasGeneratedBy ECO_0000203 NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404242.RAYl_gUhul1E7taFxTCd3j-zCUurBBdDJ-Hp1Gx192JV4130_provenance.