Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_assertion description "[We recently identified mutations of ARX in nine genotypic males with X-linked lissencephaly with abnormal genitalia (XLAG), and in several female relatives with isolated agenesis of the corpus callosum (ACC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_assertion evidence source_evidence_literature NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_assertion SIO_000772 14722918 NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_assertion wasDerivedFrom befree-20150227 NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_assertion wasGeneratedBy ECO_0000203 NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978132.RAXELwgB5gTmQCNPZb2_v5GykoDxfAdRp5_fccEAZrQhU130_provenance.