Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_assertion description "[Recombinants between VWS and both LAMB2 and DAF excluded these genes from a causal role in the etiology of VWS for the families studied in this report.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_assertion evidence source_evidence_literature NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_assertion SIO_000772 2309700 NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_assertion wasDerivedFrom befree-20150227 NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_assertion wasGeneratedBy ECO_0000203 NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP530471.RAbqTXK-rjc-2nX3JkjS0Nbs_3TZmowEDlGwX3jbmCBhQ130_provenance.