Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_assertion wasGeneratedBy ECO_0000203 NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_assertion wasDerivedFrom befree-20140225 NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_assertion SIO_000772 12107438 NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_assertion evidence source_evidence_literature NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_assertion description "[We found an IVS12+5G-->C mutation in the USHIC gene, which is associated with nonsyndromic recessive deafness ( DFNB18) segregating in the original family, S-11/12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP353938.RAD8KvgC7H52jhYfsbio62WtDTl-o5wf5m_lk3JQis-iw130_provenance.