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- source_evidence_literature type ECO_0000212 NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_assertion description "[This study confirms that TULP1 mutations cause a severe early-onset form of autosomal recessive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_assertion evidence source_evidence_literature NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_assertion SIO_000772 17620573 NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_assertion wasDerivedFrom befree-20150227 NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_assertion wasGeneratedBy ECO_0000203 NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP762089.RA3jaO3b8UsVyfM1WJtcqHIuGLWH_Yp22oxgGjSduX1_U130_provenance.