Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_assertion evidence source_evidence_literature NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_assertion SIO_000772 10852374 NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_assertion wasDerivedFrom befree-20140225 NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_assertion wasGeneratedBy ECO_0000203 NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP354285.RArjG9jMBiGD_EMWoCwK73qENrl7C6suRlUpxL91GUck0130_provenance.