Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_assertion description "[In addition, rs3825885 (NTRK3, p�=�9�נ10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p�=�2�נ10(-3)) as an OCD marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_assertion evidence source_evidence_literature NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_assertion SIO_000772 23337130 NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_assertion wasDerivedFrom befree-20150227 NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_assertion wasGeneratedBy ECO_0000203 NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600312.RAO0IU7L0KodcWR6WW81cYYssBvSrkiz8vaVu3U_ovGng130_provenance.