Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion> ?p ?o ?g. }
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- NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion type Assertion NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_head.
- NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion description "[An expanded hexanucleotide repeat in the C9ORF72 gene has recently been identified as a major cause of familial frontotemporal lobar degeneration and motor neuron disease, including cases previously identified as linked to chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_provenance.
- NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion evidence source_evidence_literature NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_provenance.
- NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion SIO_000772 22366791 NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_provenance.
- NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion wasDerivedFrom befree-20140225 NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_provenance.
- NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_assertion wasGeneratedBy ECO_0000203 NP493965.RAyuUBLi21QzLxS2YciFJ9imBYH5BHtVnjqTWCdRdkfno130_provenance.