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- source_evidence_literature type ECO_0000212 NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_assertion description "[Future studies to define the mechanism that results in the high frequency of GATA1 mutations in DS and the role of altered GATA1 in TMD and DS-AMKL will shed light on the multistep pathway in human leukemia and may lead to an increased understanding of why children with DS are markedly predisposed to leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_assertion evidence source_evidence_literature NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_assertion SIO_000772 14512321 NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_assertion wasDerivedFrom befree-2016 NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_assertion wasGeneratedBy ECO_0000203 NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.
- befree-2016 importedOn "2016-02-19" NP414765.RAjhcqXzLlUL9QIcaLQoD5lZn71Pst3_Y7VD5MqzSuChc130_provenance.