Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_assertion description "[We performed STRA6 molecular analysis in three fetuses and one child diagnosed with Matthew-Wood syndrome and in three siblings where two adult living brothers are affected with combinations of clinical anophthalmia, tetralogy of Fallot, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_assertion evidence source_evidence_literature NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_assertion SIO_000772 19309693 NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_assertion wasDerivedFrom befree-20150227 NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_assertion wasGeneratedBy ECO_0000203 NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP938259.RAORgpG95tayEDo6M0_v4X3fpXDWXXQX5_Tj-1YmZnE4I130_provenance.