Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- befree-2016 importedOn "2016-02-19" NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_assertion wasGeneratedBy ECO_0000203 NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_assertion wasDerivedFrom befree-2016 NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_assertion SIO_000772 17210889 NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_assertion evidence source_evidence_literature NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.
- NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_assertion description "[The term neuroacanthocytosis is normally used to refer to autosomal recessive chorea-acanthocytosis and X-linked McLeod syndrome, but there are other movement disorders in which erythrocyte acanthocytosis may also be seen, such as Huntington disease-like 2 and pantothenate kinase-associated neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587822.RAh_QnA23XvRQYX6pr-Pz8yQvLLRPOBHaaKFwWhxoi_7k130_provenance.