Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_assertion description "[In addition, frequencies of risk-increasing alleles at three known AMD susceptibility loci, including complement factor H (CFH), age-related maculopathy susceptibility 2 (ARMS2), and complement component 3 (C3), were evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_assertion evidence source_evidence_literature NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_assertion SIO_000772 22427542 NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_assertion wasDerivedFrom befree-2016 NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_assertion wasGeneratedBy ECO_0000203 NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.
- befree-2016 importedOn "2016-02-19" NP968621.RAx4NFfJsgDTFJwNfmyhHT4bcwE7M4DfMDI8iAlLf5_Ys130_provenance.