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- source_evidence_literature type ECO_0000212 NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_assertion description "[The expressed constructs include the intact integrin and two mutants, namely hbeta3(Y747F/Y759F) and hbeta3(S752P), each of which induces the bleeding dyscrasia, Glanzmann's thrombasthenia, in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_assertion evidence source_evidence_literature NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_assertion SIO_000772 16294265 NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_assertion wasDerivedFrom befree-20150227 NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_assertion wasGeneratedBy ECO_0000203 NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP839303.RAEOq-TYWAtpqdOxmtHXTaLpqmdjEHW9uJaELFqnKdH6E130_provenance.