Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_assertion wasGeneratedBy ECO_0000203 NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_assertion wasDerivedFrom befree-20150227 NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_assertion SIO_000772 20436471 NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_assertion evidence source_evidence_literature NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_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." NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.