Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_assertion description "[The aim of this report is precisely to describe the phenotypes of Japanese patients with novel SCN1A mutations and to reevaluate the entity of GEFS+.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_assertion evidence source_evidence_literature NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_assertion SIO_000772 11823106 NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_assertion wasDerivedFrom befree-20140225 NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_assertion wasGeneratedBy ECO_0000203 NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP515075.RAntse3CDrITuDbknOkBXgESryV6lES2Z-Zv4s2nlJmCs130_provenance.