Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_assertion wasGeneratedBy ECO_0000203 NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_assertion wasDerivedFrom gad-20130706 NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_assertion SIO_000772 20436471 NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_assertion evidence source_evidence_literature NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_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." NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.