Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_assertion description "[Analysis of TFRC1 genotypes and HFE gene mutations in French porphyria cutanea tarda (sPCT) patients revealed that, independently from HFE gene mutations, an association was found between the IVS4+198 T allele in the TFRC1 gene and sPCT patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_assertion evidence source_evidence_literature NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_assertion SIO_000772 11929045 NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_assertion wasDerivedFrom lhgdn-20090331 NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_assertion wasGeneratedBy ECO_0000203 NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193869.RAW_YYXfvwlaq14ICPx3vNzgDcL6-8yuf12-M0wlA3Qqg130_provenance.