Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_assertion description "[Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_assertion evidence source_evidence_literature NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_assertion SIO_000772 21050253 NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_assertion wasDerivedFrom befree-2016 NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_assertion wasGeneratedBy ECO_0000203 NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.
- befree-2016 importedOn "2016-02-19" NP850467.RAuvRcx7kEPRASnFv1E2nNUF_4OhGMi3fWsB7tEehGQb4130_provenance.