Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_assertion description "[Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_assertion evidence source_evidence_literature NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_assertion SIO_000772 25477152 NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_assertion wasDerivedFrom befree-2016 NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_assertion wasGeneratedBy ECO_0000203 NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245030.RAi75Y3LSFTgOJSU8PAKebuPRe1MTc0B-6X516U4a9gI4130_provenance.