Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_assertion description "[An infant with multiple anomalies and developmental delay during his first year was found to have an intersitital deletion of band p14 from the proximal short arm of chromosome 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_assertion evidence source_evidence_literature NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_assertion SIO_000772 7424912 NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_assertion wasDerivedFrom befree-20150227 NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_assertion wasGeneratedBy ECO_0000203 NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP839884.RAv-7dYY3iMWLJWXetxHpALH5ypaoC06m6INR9MfBh9sU130_provenance.