Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion description "[TNXB, FKBPL and NOTCH4 are all plausible AMD susceptibility genes, but further research will be needed to identify the causal variants and determine whether any of these genes are involved in the pathogenesis of AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion evidence source_evidence_literature NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion SIO_000772 22694956 NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion wasDerivedFrom befree-20150227 NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion wasGeneratedBy ECO_0000203 NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance.