Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_assertion description "[In addition to GCPS, Pallister-Hall syndrome (PHS; MIM 146510) and post-axial polydactyly type A (PAP-A; MIM 174200), two other disorders of human development, are caused by GLI3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_assertion evidence source_evidence_literature NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_assertion SIO_000772 10441342 NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_assertion wasDerivedFrom befree-20140225 NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_assertion wasGeneratedBy ECO_0000203 NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870776.RAFVVVjDLv5dL5Q0epWC7UFPqWedr7wK9EKbHg-XMWSw8130_provenance.