Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_assertion wasGeneratedBy ECO_0000203 NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_assertion wasDerivedFrom befree-20140225 NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_assertion SIO_000772 19615667 NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_assertion evidence source_evidence_literature NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_assertion description "[Mutations in MMP9 and MMP13 determine the mode of inheritance and the clinical spectrum of metaphyseal anadysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP604026.RAxf1PWBMY1VXB--O8GqOVuZN3LzF7VrV7Je6A7b71OdY130_provenance.