Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion> ?p ?o ?g. }
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- NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion type Assertion NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_head.
- NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion description "[Variants in the factor H gene (CFH, also known as HF1), which encodes a major inhibitor of the alternative complement pathway, are associated with the risk for developing AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_provenance.
- NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion evidence source_evidence_curated NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_provenance.
- NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion SIO_000772 16518403 NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_provenance.
- NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion wasDerivedFrom ctd_human-20150221 NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_provenance.
- NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_assertion wasGeneratedBy ECO_0000218 NP10188.RA7ceA4XsZPscYn-Go1-22LIEpAtaIJ7ZHL1LB9GDWuXA130_provenance.