Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion description "[ACTA2 mutations were identified in 16% of a cohort presenting familial TAAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion evidence source_evidence_literature NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion SIO_000772 21937134 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion wasDerivedFrom befree-20140225 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion wasGeneratedBy ECO_0000203 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.