Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_assertion description "[The exclusion of the EVC region in ATD and SRP III families suggests that locus heterogeneity exists within the short-rib dysplasia (with and without polydactyly) group of disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_assertion evidence source_evidence_literature NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_assertion SIO_000772 10951528 NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_assertion wasDerivedFrom befree-20140225 NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_assertion wasGeneratedBy ECO_0000203 NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP851632.RA_AQ0_l5Xvr1k3RhZLBTJJpRv65mwkSVRwjLWFXnnYBs130_provenance.