Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_assertion> ?p ?o ?g. }
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- NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_assertion type Assertion NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_head.
- NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_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." NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_provenance.
- NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_assertion evidence source_evidence_literature NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_provenance.
- NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_assertion SIO_000772 7534105 NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_provenance.
- NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_assertion wasDerivedFrom befree-20140225 NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_provenance.
- NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_assertion wasGeneratedBy ECO_0000203 NP477446.RAIG2F8u8PF0fg2BOnDvic6cUmFld-VPcnTUGt8mBeDXI130_provenance.