Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_assertion wasGeneratedBy ECO_0000203 NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_assertion wasDerivedFrom befree-2016 NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_assertion SIO_000772 24796371 NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_assertion evidence source_evidence_literature NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.
- NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_assertion description "[VDR Fok I, Bsm I, Apa I, and Taq I polymorphisms were genotyped using restriction fragment length polymorphism in 109 preterm infants (47 with BPD, 62 without BPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1179362.RA1DQPCZYpJr3tAiHp_IdmsuOeHCFNpzsoZ94llaTYVFQ130_provenance.