Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_assertion evidence source_evidence_literature NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_assertion SIO_000772 7585014 NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_assertion wasDerivedFrom befree-2016 NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_assertion wasGeneratedBy ECO_0000203 NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313712.RAL65UlYG3UFwSTC-RHTIGGT3Ic0eKCpO7I9MFU8ohIbQ130_provenance.