Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_assertion wasGeneratedBy ECO_0000203 NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_assertion wasDerivedFrom befree-20150227 NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_assertion SIO_000772 22894767 NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_assertion evidence source_evidence_literature NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.
- NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_assertion description "[Zellweger syndrome (ZS) is a peroxisome biogenesis disorder due to mutations in any one of 13 PEX genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619463.RA3OMu6nuXgd8Y90IU4K0LVAmAr4ql2QqWL-R100j50zs130_provenance.