Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_assertion description "[We used a series of polymorphic markers mapped to chromosome 7 to test this hypothesis in 22 children with MPS and MDS, including 19 with JCML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_assertion evidence source_evidence_literature NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_assertion SIO_000772 7534111 NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_assertion wasDerivedFrom befree-20150227 NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_assertion wasGeneratedBy ECO_0000203 NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914140.RAPK7-Bv9mjx0gLWJHEZA7ebPj2HiH_byI4hu8pywoG0I130_provenance.