Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_assertion description "[The identification of deletions associated with classic CHM or DFN3 facilitated the positional cloning of the underlying genes, REP-1 and POU3F4, respectively, and enabled the positioning of the MRX gene in between these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_assertion evidence source_evidence_literature NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_assertion SIO_000772 10644430 NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_assertion wasDerivedFrom befree-20150227 NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_assertion wasGeneratedBy ECO_0000203 NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP635686.RAiqVnq3XWEDKfivhyjve3JZ4wQW4qpSBOjV_NGsA2Ct8130_provenance.