Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP417645.RA4u56x0l2TDAV1J4zKyR_Oy6hnFPPyELDEYfmgIxhBRc130_provenance.
- 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.