Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_assertion description "[Four mutants, with deletions of 9-15 bases in the 5' regulatory region of the human interleukin 1 alpha gene, were constructed: three deleted stretches correspond to regions with high sequence similarity to regions in other genes, coding for nerve growth factor-induced proteins, e.g.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_assertion evidence source_evidence_literature NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_assertion SIO_000772 8939459 NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_assertion wasDerivedFrom befree-20140225 NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_assertion wasGeneratedBy ECO_0000203 NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP256217.RAWs29MxsJCj2Z7tSSLQ6_S7vz2sbq6K-vt3dqQLHBnKo130_provenance.