Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_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." NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_assertion evidence source_evidence_literature NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_assertion SIO_000772 19082760 NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_assertion wasDerivedFrom befree-2016 NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_assertion wasGeneratedBy ECO_0000203 NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.
- befree-2016 importedOn "2016-02-19" NP709344.RADbzTfYIagiOoRT4w-gUYBnHEjIOm_nT7I6P7UCZ6CN4130_provenance.