Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_assertion type Assertion NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_head.
- NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_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." NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_provenance.
- NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_assertion evidence source_evidence_literature NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_provenance.
- NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_assertion SIO_000772 3621643 NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_provenance.
- NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_assertion wasDerivedFrom befree-20150227 NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_provenance.
- NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_assertion wasGeneratedBy ECO_0000203 NP891218.RAh4x1Zc-ofSv5i8KBwYaPGguGbb95NfViEL77L96c7Bk130_provenance.