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- source_evidence_literature type ECO_0000212 NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_assertion wasGeneratedBy ECO_0000203 NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_assertion wasDerivedFrom gad-20150221 NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_assertion SIO_000772 19197535 NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_assertion evidence source_evidence_literature NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.
- NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_assertion description "[The frequency of the 2G allele in these subjects (46.3%) was greater than in the controls (42.0%), but less than in non-itchy dominant dystrophic EB (52.2%) or recessive dystrophic EB (62.0%), indicating that variants of a common functional polymorphism in the matrix metalloproteinase-1 gene promoter do not account for the itchy skin phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92883.RA3qzNm6uA50Adov7otgKFO52aHg1RQVWHiRzuA244t5c130_provenance.