Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_assertion evidence source_evidence_literature NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_assertion SIO_000772 11409427 NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_assertion wasDerivedFrom befree-20150227 NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_assertion wasGeneratedBy ECO_0000203 NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.