Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_assertion wasGeneratedBy ECO_0000203 NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_assertion wasDerivedFrom befree-20150227 NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_assertion SIO_000772 20730472 NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_assertion evidence source_evidence_literature NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.