Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_assertion wasGeneratedBy ECO_0000203 NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_assertion wasDerivedFrom befree-20150227 NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_assertion SIO_000772 23714752 NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_assertion evidence source_evidence_literature NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.
- NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320164.RA8KVN784frnv0opxAJTQBiFBW8cRpM8IHbVocDtkiLoI130_provenance.