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- source_evidence_literature type ECO_0000212 NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_assertion wasGeneratedBy ECO_0000203 NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_assertion wasDerivedFrom befree-2016 NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_assertion SIO_000772 24519899 NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_assertion evidence source_evidence_literature NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.
- NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_assertion description "[Likewise, cases carrying a combination of variant genotypes of CYPs and GSM1 (null) were at higher risk (up to 5-fold) of developing HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1154419.RAUIm9lI3G79M3OFeofXSqwUApgUD3fpCE-n45XOIrKPY130_provenance.