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- source_evidence_literature type ECO_0000212 NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_assertion description "[Mutations of the Wiskott-Aldrich Syndrome Protein (WASP) are responsible for classic Wiskott-Aldrich Syndrome (WAS), X-linked thrombocytopenia (XLT), and in rare instances congenital X-linked neutropenia (XLN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_assertion evidence source_evidence_literature NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_assertion SIO_000772 19082760 NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_assertion wasDerivedFrom befree-20150227 NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_assertion wasGeneratedBy ECO_0000203 NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776700.RAHRt8asLS4sTNFs35m16EHa1Z4Q67Jbgw7ri1u-P12r8130_provenance.