Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_assertion description "[In humans, mutations in TMEM67 (also known as MKS3) cause both MKS and JBTS, with TMEM67 encoding the orphan receptor meckelin (TMEM67) that localizes to the ciliary transition zone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_assertion evidence source_evidence_literature NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_assertion SIO_000772 23283079 NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_assertion wasDerivedFrom befree-20150227 NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_assertion wasGeneratedBy ECO_0000203 NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960756.RAwI9NQa9QayqvMFgkZJlmGMplvr0UJXVRY3BGhBs8bKk130_provenance.