Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_assertion description "[Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_assertion evidence source_evidence_literature NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_assertion SIO_000772 18192287 NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_assertion wasDerivedFrom befree-2016 NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_assertion wasGeneratedBy ECO_0000203 NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.
- befree-2016 importedOn "2016-02-19" NP649607.RAC9k_tbG6TUXWq3cYr1ZPCiLviIlb0C7M2VvKnEg71CA130_provenance.