Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_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." NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_assertion evidence source_evidence_literature NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_assertion SIO_000772 10852374 NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_assertion wasDerivedFrom befree-20150227 NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_assertion wasGeneratedBy ECO_0000203 NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784068.RASv5F2FpgMjhpXJzjPqfCXJAxft_26818EZqVdi0mGOE130_provenance.