Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion description "[C596G mutation in FBN1 causes Marfan syndrome with exotropia in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion evidence source_evidence_literature NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion SIO_000772 25729264 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion wasDerivedFrom befree-2016 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion wasGeneratedBy ECO_0000203 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.