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- source_evidence_literature type ECO_0000212 NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_assertion description "[Alport syndrome (ATS) is a type-IV collagen inherited disorder, caused by mutations in COL4A3 and COL4A4 (autosomal recessive) or COL4A5 (X-linked).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_assertion evidence source_evidence_literature NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_assertion SIO_000772 23144074 NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_assertion wasDerivedFrom befree-20140225 NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_assertion wasGeneratedBy ECO_0000203 NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP784610.RAD5CqOMz7qM0V5Wrj7s7I0C5Vmo4B-b3wilbYQopIU3E130_provenance.