Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_assertion description "[Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare heritable disorder of connective tissue characterized by congenital malformations of the great toes and recurrent episodes of painful soft tissue swelling that lead to heterotopic ossifications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_assertion evidence source_evidence_literature NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_assertion SIO_000772 19300893 NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_assertion wasDerivedFrom befree-20140225 NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_assertion wasGeneratedBy ECO_0000203 NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311966.RAgL2oQn_cSwRCClfHqHJUhtPR_o3V4_rp553oElgfIFY130_provenance.