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- source_evidence_literature type ECO_0000212 NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_assertion description "[To better define the deleted chromosomal loci and understand the genetic instability in EC tissues, we selected 12 microsatellite markers (D3S1232, D3S1238, D3S1289, D3S1480, D3S647, D3S966, D3S1317, D3S659, D9S156, D9S171, D9S176 and GSN) to examine 36 paired EC tissues for loss of heterozygosity (LOH) and microsatellite instability (MIN) on chromosomes 3 and 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_assertion evidence source_evidence_literature NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_assertion SIO_000772 8637728 NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_assertion wasDerivedFrom befree-20140225 NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_assertion wasGeneratedBy ECO_0000203 NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP207296.RA1Eokc7VfwVBShFTzlFaNkeymRSomXSErkO5avtRtD9c130_provenance.