Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion> ?p ?o ?g. }
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- NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion type Assertion NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_head.
- NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion description "[We report a patient with myelodysplastic syndrome (refractory anemia) showing the karyotype 46,XY,+1,der(1;10)(q10;p10), resulting in trisomy 1q and monosomy 10q abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_provenance.
- NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion evidence source_evidence_literature NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_provenance.
- NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion SIO_000772 17213027 NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_provenance.
- NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion wasDerivedFrom befree-20140225 NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_provenance.
- NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_assertion wasGeneratedBy ECO_0000203 NP782923.RARM7Me2BfPql6NcQ0DpLbdkYp7KzQoTc-7thZF_F8trs130_provenance.