Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion> ?p ?o ?g. }
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- NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion type Assertion NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_head.
- 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.