Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_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." NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_assertion evidence source_evidence_literature NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_assertion SIO_000772 18177646 NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_assertion wasDerivedFrom befree-20140225 NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_assertion wasGeneratedBy ECO_0000203 NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP906978.RA2zLMKRGOJ4fL9zP3UpJnZQvHjZ7u1724dw6TNwMK11k130_provenance.