Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_assertion evidence source_evidence_literature NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_assertion SIO_000772 19182766 NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_assertion wasDerivedFrom befree-20150227 NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_assertion wasGeneratedBy ECO_0000203 NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.