Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_assertion description "[Mutations in the fibrillin gene on chromosome 15 (FBN1) were described at first in the heritable connective tissue disorder, Marfan syndrome (MFS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_assertion evidence source_evidence_literature NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_assertion SIO_000772 8594563 NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_assertion wasDerivedFrom befree-20140225 NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_assertion wasGeneratedBy ECO_0000203 NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.
- befree-20140225 importedOn "2014-02-25" NP459930.RA2rH7GxZM1hCwfzWBk0krWTfbcrPEm0G4WzWRIrX98Ds130_provenance.