Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_assertion description "[The genes for phosphatidylinositol transfer protein (PITPN), retinal guanylate cyclase (GUC2D), beta-arrestin 2 (ARRB2), pigment epithelium-derived factor (PEDF) and recoverin (RCV1) map to this region and are candidate genes for retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_assertion evidence source_evidence_literature NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_assertion SIO_000772 8733141 NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_assertion wasDerivedFrom befree-20150227 NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_assertion wasGeneratedBy ECO_0000203 NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668444.RAH67DQyRjva74tVHDaxSAE6y_cEi31SBeBKS0fH9wtLs130_provenance.