Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_assertion description "[A control subject with NPHP and with a homozygous NPHP1 deletion was also identified, retrospectively, as having a mild MTS and borderline intelligence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_assertion evidence source_evidence_literature NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_assertion SIO_000772 15138899 NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_assertion wasDerivedFrom befree-20140225 NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_assertion wasGeneratedBy ECO_0000203 NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP309197.RAn-aDIljmNcrXRBYPIGOa59I8B0fxQfPZCE3p1LMUe9E130_provenance.