Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_assertion> ?p ?o ?g. }
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- NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_assertion type Assertion NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_head.
- NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_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." NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_provenance.
- NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_assertion evidence source_evidence_literature NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_provenance.
- NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_assertion SIO_000772 3621643 NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_provenance.
- NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_assertion wasDerivedFrom befree-20140225 NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_provenance.
- NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_assertion wasGeneratedBy ECO_0000203 NP377690.RAzAu1au3umkJucfo9fW-yz-Ee8uu8lQFR5o6zVl-Cr2w130_provenance.