Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- befree-2016 importedOn "2016-02-19" NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_assertion wasGeneratedBy ECO_0000203 NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_assertion wasDerivedFrom befree-2016 NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_assertion SIO_000772 1868037 NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_assertion evidence source_evidence_literature NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.
- NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_assertion description "[Chromosome 10 exhibited a complex deletion pattern with terminal deletions of the p or the q arm (2 cases each), a deletion pattern that could be interpreted as nonreciprocal translocations of the q arm (2 cases), or allelic losses on all informative loci, suggesting monosomy (2 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686071.RAhm6VOaxFwr3MUsmQ8wA2-pWAzW3-D4Wufb_gXhSBtJI130_provenance.