Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_assertion description "[We examined our patient population with episodic ataxia and hemiplegic migraine but with no mutation in either CACNA1A or ATP1A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_assertion evidence source_evidence_literature NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_assertion SIO_000772 16116111 NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_assertion wasDerivedFrom befree-20150227 NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_assertion wasGeneratedBy ECO_0000203 NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256069.RApOZjQKGGkf_CXiYLogO1al14NXpApjUP8HoAKXwQwxY130_provenance.