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- source_evidence_literature type ECO_0000212 NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- befree-2016 importedOn "2016-02-19" NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_assertion wasGeneratedBy ECO_0000203 NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_assertion wasDerivedFrom befree-2016 NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_assertion SIO_000772 22534615 NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_assertion evidence source_evidence_literature NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.
- NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_assertion description "[In this family, a T613M mutation in the ATP1A3 gene was confirmed, the most common mutation present in patients with RDP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977587.RAebYvy4t-ZnJRlsXlWX7do4jifznEDFW3-H30RUESQdw130_provenance.