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- NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_assertion type Assertion NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_head.
- NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_assertion description "[Clinical reanalysis indicated co-ocurrence of two different phenotypes in the same family: Bardet-Biedl syndrome in the individual harboring the BBS1 mutation and non-syndromic arRP in extended family members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_provenance.
- NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_assertion evidence source_evidence_literature NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_provenance.
- NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_assertion SIO_000772 25494902 NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_provenance.
- NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_assertion wasDerivedFrom befree-2016 NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_provenance.
- NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_assertion wasGeneratedBy ECO_0000203 NP1246809.RA9CjxL7UhRFl0hpo_R01AhqIDD51vvo_y19kOf4wExA4130_provenance.