Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_assertion description "[Germline GATA2 mutations are involved in a group of complex syndromes with overlapping clinical features of immune deficiency, lymphedema and propensity to acute myeloid leukemia or myelodysplastic syndrome (AML-MDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_assertion evidence source_evidence_literature NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_assertion SIO_000772 24754962 NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_assertion wasDerivedFrom befree-20150227 NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_assertion wasGeneratedBy ECO_0000203 NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418956.RAw7AfTTIwQEvSRTPNvpG5i0NCDSKigyqP-mGbNxntLj8130_provenance.