Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_assertion wasGeneratedBy ECO_0000203 NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_assertion wasDerivedFrom befree-20140225 NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_assertion SIO_000772 9915945 NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_assertion evidence source_evidence_literature NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_assertion description "[A Prader-Willi syndrome patient is described who has a de novo balanced translocation, (4;15)(q27;q11.2)pat, with breakpoints lying between SNRPN exons 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP252051.RAltM2ImJhKphk2LDSAsAFYViIwJTuyhF8VYsIcxCe4jQ130_provenance.