Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_assertion description "[Contribution of RET, NTRK3 and EDN3 to the expression of Hirschsprung disease in a multiplex family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_assertion evidence source_evidence_literature NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_assertion SIO_000772 19556619 NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_assertion wasDerivedFrom befree-2016 NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_assertion wasGeneratedBy ECO_0000203 NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.
- befree-2016 importedOn "2016-02-19" NP747583.RA661z6E3p7phC0k_SJ0acFc4hIFH6RsJMiwvvO_dBK9c130_provenance.