Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_assertion description "[SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_assertion evidence source_evidence_literature NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_assertion SIO_000772 15944908 NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_assertion wasDerivedFrom befree-20150227 NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_assertion wasGeneratedBy ECO_0000203 NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682512.RAAeMP_kzwMMbI88gu1eWUPJuPZgQmDFF1v1I0qEB3NY0130_provenance.