Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_assertion wasGeneratedBy ECO_0000203 NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_assertion wasDerivedFrom befree-20140225 NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_assertion SIO_000772 18060736 NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_assertion evidence source_evidence_literature NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_assertion description "[In the second patient, a female with mental retardation and ectodermal dysplasia and a balanced translocation, t(X;9) (q13.1;p24), we mapped the 9p24 breakpoint to a region overlapping with the centromeric end of the 230-kb subtelomeric deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP758947.RAzG2OkM4GQd2EVZmRUy9WRN2FnOWc5liistOXv_EMtL4130_provenance.