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- source_evidence_literature type ECO_0000212 NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_assertion description "[A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_assertion evidence source_evidence_literature NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_assertion SIO_000772 25496299 NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_assertion wasDerivedFrom befree-2016 NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_assertion wasGeneratedBy ECO_0000203 NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246907.RA2Rn3_Wi1pItALT1-w8uaMwtpOe7I2czaR6SmBJGEkPk130_provenance.