Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_assertion evidence source_evidence_literature NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_assertion SIO_000772 10424820 NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_assertion wasDerivedFrom befree-20140225 NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_assertion wasGeneratedBy ECO_0000203 NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.