Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_assertion description "[We also screened 408 sporadic patients with CHDs and identified a case with ASD and a 17-bp deletion in ACTC1 predicting a non-functional protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_assertion evidence source_evidence_literature NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_assertion SIO_000772 17947298 NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_assertion wasDerivedFrom befree-20140225 NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_assertion wasGeneratedBy ECO_0000203 NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.
- befree-20140225 importedOn "2014-02-25" NP796880.RA3aibFVBe0Mq6SB9xpsvBapIc3ssEYSKRmzITWN5e6Go130_provenance.