Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_assertion evidence source_evidence_literature NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_assertion SIO_000772 8227344 NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_assertion wasDerivedFrom befree-20140225 NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_assertion wasGeneratedBy ECO_0000203 NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.