Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion wasGeneratedBy ECO_0000203 NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion wasDerivedFrom befree-20150227 NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion SIO_000772 24634231 NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion evidence source_evidence_literature NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.
- NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion description "[ISL1 is related to the atrial septal defect group and the ventricular septal defect group, and the genotypes were associated with the occurrence of CHD in the dominant mode of inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance.