Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_assertion wasGeneratedBy ECO_0000218 NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_assertion wasDerivedFrom ctd_human-20150221 NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_assertion SIO_000772 20436471 NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_assertion evidence source_evidence_curated NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.