Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion> ?p ?o ?g. }
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- NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion type Assertion NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_head.
- NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion description "[Here we have analyzed a balanced t(11;16)(p15;q13) chromosomal translocation associated with the BWS phenotype and mapped the breakpoint positions for both chromosomes 11 and 16 by using somatic cell hybrids and polymorphic markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_provenance.
- NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion evidence source_evidence_literature NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_provenance.
- NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion SIO_000772 7534105 NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_provenance.
- NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion wasDerivedFrom befree-20140225 NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_provenance.
- NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_assertion wasGeneratedBy ECO_0000203 NP838912.RA4C-un_LxVWKhpp2fYF3b_Tw-lnTd7ADwCy6f2wnLC2k130_provenance.