Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_assertion description "[Uniparental disomy (UPD) of single chromosomes is a well-known molecular aberration in a group of congenital diseases commonly known as imprinting disorders (IDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_assertion evidence source_evidence_literature NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_assertion SIO_000772 23188046 NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_assertion wasDerivedFrom befree-20140225 NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_assertion wasGeneratedBy ECO_0000203 NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP599756.RAefPVxO0gyuNnKE83oAJgpdMRvA0Kn0ns4SD-ehDwUqw130_provenance.