Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_assertion description "[The enamel-renal syndrome of amelogenesis imperfecta (AI) and nephrocalcinosis, and the amelogenesis imperfecta-gingival fibromatosis syndrome have both been associated with mutations in FAM20A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_assertion evidence source_evidence_literature NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_assertion SIO_000772 24259279 NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_assertion wasDerivedFrom befree-2016 NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_assertion wasGeneratedBy ECO_0000203 NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1130049.RAyn2kyKTADMjc3NGB6W2WAyRP23nQrLysNE2X9j9jKXI130_provenance.