Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion description "[FBN1 mutations typically cause the Marfan syndrome, an autosomal dominant disorder manifesting with skeletal overgrowth, aortic aneurysm, and lens dislocation (ectopia lentis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion evidence source_evidence_literature NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion SIO_000772 21858451 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion wasDerivedFrom befree-2016 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion wasGeneratedBy ECO_0000203 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- befree-2016 importedOn "2016-02-19" NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.