Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_assertion description "[Cerebellar malformations consistent with the MTS may be relatively common in patients with juvenile NPHP without classic symptoms of JS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_assertion evidence source_evidence_literature NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_assertion SIO_000772 15138899 NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_assertion wasDerivedFrom befree-20140225 NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_assertion wasGeneratedBy ECO_0000203 NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.
- befree-20140225 importedOn "2014-02-25" NP842648.RA_r5TeCZC_YE00zRtL1Ov4TlM68Nu5i2Nz21uEgymO58130_provenance.