Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_assertion wasGeneratedBy ECO_0000203 NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_assertion wasDerivedFrom befree-20150227 NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_assertion SIO_000772 10814714 NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_assertion evidence source_evidence_literature NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.
- NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_assertion description "[We have examined the mutational status of the GPC3 and GPC4 genes in one patient with Perlman syndrome, three patients with overgrowth without syndrome diagnosis, ten unrelated SGBS-patients and 11 BWS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397965.RAr2xfPWqD7xh4vGi_JbDMjKYSItY-LSsIoVlmba837t4130_provenance.