Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_assertion description "[These data suggested that AML1 point mutation is one of the major driving forces of MDS/AML, and these mutations may represent a distinct clinicopathologic-genetic entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_assertion evidence source_evidence_literature NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_assertion SIO_000772 14615365 NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_assertion wasDerivedFrom befree-2016 NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_assertion wasGeneratedBy ECO_0000203 NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.
- befree-2016 importedOn "2016-02-19" NP420585.RAdJJrm9LbVWSUtNJd0Q7RnRcKEgTIKA1G-8Pf_VDrOGA130_provenance.