Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_assertion description "[Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_assertion evidence source_evidence_literature NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_assertion SIO_000772 18805828 NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_assertion wasDerivedFrom befree-20140225 NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_assertion wasGeneratedBy ECO_0000203 NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP549782.RALdEonX_6eIEW3-8mSWRxTqOiGmA_Z2xXGePtkYcwzG8130_provenance.