Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_assertion description "[A similar issue of differential diagnosis was raised by a large 4.3 Mb 2q22.3q23.1 deletion encompassing ZEB2, the gene responsible for the Mowat-Wilson syndrome, whose signs may overlap with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_assertion evidence source_evidence_literature NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_assertion SIO_000772 20125191 NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_assertion wasDerivedFrom befree-20150227 NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_assertion wasGeneratedBy ECO_0000203 NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831109.RAF7HcDMOlFnc6beo7pdu9Gmvt2LdL_9klUsRhJf66w-8130_provenance.