Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- befree-2016 importedOn "2016-02-19" NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_assertion wasGeneratedBy ECO_0000203 NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_assertion wasDerivedFrom befree-2016 NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_assertion SIO_000772 22219654 NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_assertion evidence source_evidence_literature NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.
- NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_assertion description "[The 25 CNVs were not located at known chromosomal loci for PCG, namely GLC3A, which harbors CYP1B1 (2p21), GLC3B (1p36.2-p36.1), or GLC3C (14q23), and did not include any target genes associated with PCG or anterior segmental dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951032.RAjFNzMakbjelg2OG1G2HKdBx2wcaxYyKoJInJtoqoVGY130_provenance.