Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_assertion description "[Although ranked among the least common congenital heart defects, TA provides an excellent model for the role of individual genes in cardiac morphogenesis as exemplified by TBX1 deficiency caused by point mutations or, more commonly, hemizygosity as part of the 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_assertion evidence source_evidence_literature NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_assertion SIO_000772 25713110 NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_assertion wasDerivedFrom befree-2016 NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_assertion wasGeneratedBy ECO_0000203 NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266162.RA0g5ajaFf41IOR6q6ALTW_vS3c-LlGGxlMHOsutBkviw130_provenance.