Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_assertion evidence source_evidence_literature NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_assertion SIO_000772 17665217 NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_assertion wasDerivedFrom befree-2016 NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_assertion wasGeneratedBy ECO_0000203 NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- befree-2016 importedOn "2016-02-19" NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.