Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion type Assertion NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_head.
- NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion description "[We report an infant with holoprosencephaly (HPE), sacral anomalies, and situs ambiguus with a 46,XY,der(7)t(2;7)(p23.2;q36.1) karyotype as a result of an adjacent-1 segregation of a t(2;7)pat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion evidence source_evidence_literature NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion SIO_000772 10852374 NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion wasDerivedFrom befree-20140225 NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_assertion wasGeneratedBy ECO_0000203 NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.