Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion> ?p ?o ?g. }
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- NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion type Assertion NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_head.
- NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion description "[Some features of GPS[+] overlap with Stargardt disease (STGD1), a recessive macular dystrophy caused by biallelic sequence variants in the ATP-binding cassette transporter 4 (ABCA4) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_provenance.
- NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion evidence source_evidence_literature NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_provenance.
- NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion SIO_000772 22427542 NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_provenance.
- NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion wasDerivedFrom befree-20150227 NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_provenance.
- NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_assertion wasGeneratedBy ECO_0000203 NP218941.RAg-XNgoRZ11iv0xpwzAnjBawFXQx2k5Lsdo-gJKdSJ6g130_provenance.