Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_assertion description "[In two cases of SDS with bone marrow failure and isolated del(20q) interphase fluorescence in situ hybridization (I-FISH) found no abnormalities in FHIT/3p14.2, IKZF1/7p13, D7S486/7q31, PTEN/10q23.3, WT1/11p13, ATM/11q23, D13S25/13q14, TP53/17p13, NF1/17q11, SMAD2/18q21, RUNX1/21q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_assertion evidence source_evidence_literature NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_assertion SIO_000772 19016724 NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_assertion wasDerivedFrom befree-20150227 NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_assertion wasGeneratedBy ECO_0000203 NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411576.RAlBTz-e5VREwWM_Q48RXAYEm2ldqoF_8X8AcQqUo42ik130_provenance.