Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- befree-2016 importedOn "2016-02-19" NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_assertion wasGeneratedBy ECO_0000203 NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_assertion wasDerivedFrom befree-2016 NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_assertion SIO_000772 9373191 NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_assertion evidence source_evidence_literature NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.
- NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_assertion description "[The human thrombin receptor gene has been localized to band q13 of chromosome 5, a site that is at or contiguous to the common proximal breakpoint found in the majority of patients with interstitial deletions involving 5q (5q- syndrome; refractory anemia with dysmegakaryocytopoiesis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1384186.RA3GQmFEq2a8voObhqO7jFN35lYrVeo2j7KhUdb8JoZis130_provenance.