Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_assertion description "[Together, the group of phenotypes associated with ARX mutations demonstrates remarkable pleiotropy, but also comprises a nearly continuous series of developmental disorders that begins with hydranencephaly, lissencephaly, and agenesis of the corpus callosum, and ends with a series of overlapping syndromes with apparently normal brain structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_assertion evidence source_evidence_literature NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_assertion SIO_000772 14722918 NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_assertion wasDerivedFrom befree-20140225 NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_assertion wasGeneratedBy ECO_0000203 NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP804910.RAmWRaIEZ2UxaOdjx--1arBem4KkTBowJ9dZIEq2i_4Oc130_provenance.