Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_assertion description "[Compared to PLEKHA1, HTRA1/LOC387715 genetic variations were independently and strongly associated with exudative AMD in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_assertion evidence source_evidence_literature NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_assertion SIO_000772 18079691 NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_assertion wasDerivedFrom gad-20150221 NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_assertion wasGeneratedBy ECO_0000203 NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP66455.RAvfDHDZAJmh724vNIP32xM1yqx_7Sx1QKHbhgCObI6EM130_provenance.