Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_assertion wasGeneratedBy ECO_0000203 NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_assertion wasDerivedFrom befree-20140225 NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_assertion SIO_000772 1773535 NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_assertion evidence source_evidence_literature NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_assertion description "[All of them have a balanced reciprocal translocation (46,XY or XX, t(7;9) (q11.21;p12) or (46,XY or XX, t(7;9) (p11.2;q12)), but no other members of the family have either the EEC syndrome or chromosome abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP837930.RANfKpWWu1AL73hYQBMvTjWCfz6HJMUwo4rY5uqkGKwPo130_provenance.