Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion description "[The study focused on the associated brain malformations, including neuronal migration defects, which predominated in individuals with ZIC2 mutations, and neural tube defects, which were frequently associated with ZIC2 (rachischisis) and TGIF mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion evidence source_evidence_literature NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion SIO_000772 21940735 NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion wasDerivedFrom befree-20140225 NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion wasGeneratedBy ECO_0000203 NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance.