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- source_evidence_literature type ECO_0000212 NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_assertion description "[We have identified 11 different previously unreported mutations in ALOX12B and ALOXE3 in 21 ARCI patients from 19 unrelated families and demonstrated that mutations in the two genes are the second most common cause for ARCI in this cohort of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_assertion evidence source_evidence_literature NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_assertion SIO_000772 19131948 NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_assertion wasDerivedFrom befree-20140225 NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_assertion wasGeneratedBy ECO_0000203 NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP765086.RA0PwkWPoZo7bIFT1aauafadXoXIEMZ3N7B90HNu1USe4130_provenance.