Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_assertion description "[A 5-month-old girl had a typical 12p trisomy syndrome due to a monocentric i(12p) present in a 46-chromosome complement that also included the translocation of all 12q onto the 8p telomere; i.e., her complex karyotype could be written as 46,XX,-8,-12, +der(8),t(8;12)(p23.3;cen),+i(12p).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_assertion evidence source_evidence_literature NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_assertion SIO_000772 3621643 NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_assertion wasDerivedFrom befree-20140225 NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_assertion wasGeneratedBy ECO_0000203 NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP441759.RAV0r5Ai5MfO53_gz9SNBoZoP1qlUBx8b8_TCXL6p22Tw130_provenance.