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- NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_assertion type Assertion NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_head.
- NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_assertion wasGeneratedBy ECO_0000203 NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_assertion wasDerivedFrom befree-20150227 NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_assertion SIO_000772 24211322 NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_assertion evidence source_evidence_literature NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_assertion description "[Homozygosity mapping identifies a GALK1 mutation as the cause of autosomal recessive congenital cataracts in 4 adult siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.