Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion> ?p ?o ?g. }
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- NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_assertion type Assertion NP615078.RA11oGdEMHtzrrkCDD1DDTyaO35kTq9l416bWn0NTfMz0130_head.
- 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.