Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_assertion description "[These discrepancies were compounded with the finding of RPGR mutations leading exclusively to X-linked cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_assertion evidence source_evidence_literature NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_assertion SIO_000772 12140192 NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_assertion wasDerivedFrom befree-2016 NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_assertion wasGeneratedBy ECO_0000203 NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP362499.RA1m0W4Xh23rrQVeq7aouBnyB6C_tGCoUy5Cqmj_TthQ4130_provenance.