Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion description "[The common variant in the human complement Factor H gene (CFH), with Tyr402His, is linked to age-related macular degeneration (AMD), a prevalent disorder leading to visual impairment and irreversible blindness in elderly patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion evidence source_evidence_literature NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion SIO_000772 17399790 NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion wasDerivedFrom befree-20140225 NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion wasGeneratedBy ECO_0000203 NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_provenance.