Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_assertion description "[Attempting to replicate the reported data, we evaluated allele-specific expression of DLX5 and DLX6 in mouse x human somatic cell hybrids, lymphoblastoid cell lines, and frontal cortex from controls and individuals with MECP2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_assertion evidence source_evidence_literature NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_assertion SIO_000772 17701895 NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_assertion wasDerivedFrom befree-20140225 NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_assertion wasGeneratedBy ECO_0000203 NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223755.RAyVIY3t4xMSv81TIMH3dzccKfekT-ZLNkIwotEy5w7iA130_provenance.