Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_assertion description "[A mouse model that recapitulates X-linked lissencephaly with ambiguous genitalia (XLAG) is far from elucidating the substrate for phenotypes that different ARX mutations cause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_assertion evidence source_evidence_literature NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_assertion SIO_000772 21426321 NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_assertion wasDerivedFrom befree-2016 NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_assertion wasGeneratedBy ECO_0000203 NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.
- befree-2016 importedOn "2016-02-19" NP881481.RAWWVu1QV5OcdbzR4JTfTUpojlt-QMeYx9Mb8D_gw-RB0130_provenance.