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- source_evidence_literature type ECO_0000212 NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_assertion description "[X-ray repair cross-complementing group 4 (XRCC4) promoter -1394( *)T-related genotype, but not XRCC4 codon 247/intron 3 or xeroderma pigmentosum group D codon 312, 751/promoter -114, polymorphisms are correlated with higher susceptibility to myoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_assertion evidence source_evidence_literature NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_assertion SIO_000772 18177646 NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_assertion wasDerivedFrom befree-2016 NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_assertion wasGeneratedBy ECO_0000203 NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.
- befree-2016 importedOn "2016-02-19" NP648531.RAq5g--NGJ3OVb8RdIMuNMorh8lyO5yrLjYnAAlTaZELM130_provenance.