Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_assertion description "[Absence of TNX mRNA and protein in the proband, mapping of the TNX gene and HLA typing of this family suggest recessive inheritance of TNX deficiency and connective-tissue disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_assertion evidence source_evidence_literature NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_assertion SIO_000772 9288108 NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_assertion wasDerivedFrom befree-2016 NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_assertion wasGeneratedBy ECO_0000203 NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1380030.RAEs2VQUJm2YIhvvcTfiDcWX23vmnI-aebpWGjxWMUFLw130_provenance.