Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion description "[The contribution of copy number variation (CNV) to specific congenital heart disease (CHD) phenotypes including AVSD is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion evidence source_evidence_literature NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion SIO_000772 22529060 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion wasDerivedFrom befree-2016 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion wasGeneratedBy ECO_0000203 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- befree-2016 importedOn "2016-02-19" NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.