Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_assertion wasGeneratedBy ECO_0000203 NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_assertion wasDerivedFrom befree-2016 NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_assertion SIO_000772 23227268 NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_assertion evidence source_evidence_literature NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.
- NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_assertion description "[Mutations in MSX1, PAX9, AXIN2, EDA and WNT10A can cause non-syndromic familial tooth agenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1034977.RAVRy4SSHb7mL9j9ijDF5907m-zM22FFjwmCv6eqd1ZCw130_provenance.