Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_assertion description "[EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_assertion evidence source_evidence_curated NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_assertion SIO_000772 24292273 NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_assertion wasDerivedFrom ctd_human-2016 NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_assertion wasGeneratedBy ECO_0000218 NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP33664.RAAFL79rvz0dIVgXdBjYDYln4jkWxRYDWHG9cWLnv06kQ130_provenance.