Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- 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.
- NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_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." NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.