Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_assertion description "[We assessed a family in which the translocation between chromosomes 12 and 16 segregates; one of the eight progenies with the karyotype 47,XY,+21,t(12;16)(q24;q24) was heterozygote for the translocation and presented with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_assertion evidence source_evidence_literature NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_assertion SIO_000772 18990986 NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_assertion wasDerivedFrom befree-2016 NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_assertion wasGeneratedBy ECO_0000203 NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.
- befree-2016 importedOn "2016-02-19" NP702182.RA4zs5qfzLWDLV-2ooK73fSs0XIamOy3srqwjHi2BMGi4130_provenance.