Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_assertion description "[We screened 176 German patients with albinism for mutations within the MATP gene and identified five individuals with OCA4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_assertion evidence source_evidence_curated NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_assertion SIO_000772 14722913 NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_assertion wasDerivedFrom uniprot-20150221 NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_assertion wasGeneratedBy ECO_0000218 NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP5084.RAhK8mVfa66sCw6S9iRoL4UDHppVv6jy-U3ENB10RQifI130_provenance.