Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_assertion description "[While double knockout of Dlx5 and Dlx6 resulted in limb defects in mice, the majority of patients with SHFM1 had only heterozygous chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_assertion evidence source_evidence_literature NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_assertion SIO_000772 25332435 NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_assertion wasDerivedFrom befree-2016 NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_assertion wasGeneratedBy ECO_0000203 NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231037.RAWZ6BPdl_lvfbtTdOQVmj2-p9Nxs5CZq-a6fnfdklfEc130_provenance.