Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_assertion description "[Case 1 involved a 17-year-old with severe MR, profound deafness and dysmorphic features with reciprocal translocation t(3;7)(q26.2; p15.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_assertion evidence source_evidence_literature NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_assertion SIO_000772 16131774 NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_assertion wasDerivedFrom befree-20140225 NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_assertion wasGeneratedBy ECO_0000203 NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP617289.RAeGgZtpcMJKLt9AWCSnpHae1CdGeK05B-btD3w7MKS6c130_provenance.