Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_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." NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_assertion evidence source_evidence_literature NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_assertion SIO_000772 14722918 NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_assertion wasDerivedFrom befree-20150227 NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_assertion wasGeneratedBy ECO_0000203 NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835551.RAdp34960LYwTxv_MRQcm5rwQOEBDLNPAvV8FtlHkSpBo130_provenance.