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- source_evidence_literature type ECO_0000212 NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- befree-2016 importedOn "2016-02-19" NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_assertion wasGeneratedBy ECO_0000203 NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_assertion wasDerivedFrom befree-2016 NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_assertion SIO_000772 22408652 NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_assertion evidence source_evidence_literature NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.
- NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_assertion description "[Nearly all cases of FOP are caused by the identical mutation in the ACVR1 gene that causes a single amino acid substitution, R206H, in the bone morphogenetic protein (BMP) type I receptor ACVR1 (formerly known as ALK2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966994.RADBjwpiKYW2yzx83M1GoAzbbGNAWMRP71k1le2gKug8s130_provenance.