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- source_evidence_literature type ECO_0000212 NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- befree-2016 importedOn "2016-02-19" NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_assertion wasGeneratedBy ECO_0000203 NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_assertion wasDerivedFrom befree-2016 NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_assertion SIO_000772 22739344 NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_assertion evidence source_evidence_literature NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.
- NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_assertion description "[We believe that the FOXG1 gene should be considered in severely mentally retarded patients (no speech-language) with severe acquired microcephaly (-4 to-6 SD) and few clinical features suggestive of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993580.RARNM7d4M2FlOQ1BGNIWK7erbDtd6adDJD53LPDwmNBFE130_provenance.