Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP377012.RAfUWX6abk_S3xAACpRYvKK1rFS9MGHdx4SBUe_NGYW7E130_provenance.