Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_assertion description "[We progressively screened DNA samples from 613 individuals with ID initially for the most frequent ARX mutations (c.304ins(GCG)(7)'expansion' of pA1 and c.429_452dup 'dup24bp' of pA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_assertion evidence source_evidence_literature NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_assertion SIO_000772 21496008 NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_assertion wasDerivedFrom befree-20140225 NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_assertion wasGeneratedBy ECO_0000203 NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP736763.RAX-mWmP6oUXKNnfN9SlWkKhDTlKL4YlMHFDsvHF2XKbU130_provenance.