Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion description "[Somatic, heterozygous ASXL1 mutations were identified in 14/48 (29%) of patients with GATA2 deficiency, including four out of five patients who developed a proliferative chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion evidence source_evidence_literature NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion SIO_000772 24077845 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion wasDerivedFrom befree-2016 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion wasGeneratedBy ECO_0000203 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.